Category: 153719-23-4

Reference of 153719-23-4, An article , which mentions 153719-23-4, molecular formula is C8H10ClN5O3S. The compound – N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide played an important role in people’s production and life.

The invention discloses a new smoke alkali containing spiromesifen the insecticidal composition, containing as an active ingredient a A and the active ingredient is insecticidal composition B, wherein the active ingredient is selected from A spiromesifen, B an active ingredient a compound selected from the following: thiamethoxam, thiacloprid, clothianidine, dinotefuran, and the active ingredient with the active ingredient A the weight ratio of B […] 1 […] 60-80 1. The compositions of the invention against agricultural production a plurality of pest with synergistic effect, reduces the dosage of pesticide, reduced the level of residue on the crop of agricultural chemicals, reduce the environmental pollution, safety to people and animals, good environmental compatibility, the pest is difficult to produce drug resistance. (by machine translation)

The invention discloses a new smoke alkali containing spiromesifen the insecticidal composition, containing as an active ingredient a A and the active ingredient is insecticidal composition B, wherein the active ingredient is selected from A spiromesifen, B an active ingredient a compound selected from the following: thiamethoxam, thiacloprid, clothianidine, dinotefuran, and the active ingredient with the active ingredient A the weight ratio of B […] 1 […] 60-80 1. The compositions of the invention against agricultural production a plurality of pest with synergistic effect, reduces the dosage of pesticide, reduced the level of residue on the crop of agricultural chemicals, reduce the environmental pollution, safety to people and animals, good environmental compatibility, the pest is difficult to produce drug resistance. (by machine translation)

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Reference£º
Thiazole | C3H8850NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route of 153719-23-4. Let¡¯s face it, organic chemistry can seem difficult to learn. Especially from a beginner¡¯s point of view. Like 153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide. In a document type is Patent, introducing its new discovery.

A combination, suitable for agricultural use comprising (I) a compound of formula (X) and (II) one or more agents selected, independently of each other, from any one of (A) to (G): (A) a certain fungicide; (B) a certain insecticide or nematicide; (C) a certain protein produced by the plant pathogenic bacterium, Erwinia amylovora; (D) a certain biological strain, (E) a certain Isoflavone; (F) a plant growth regulator; and (G) a plant activator, such as acibenzolar-S-methyl, wherein compound of formula (X) is a mixture of (formulas)

A combination, suitable for agricultural use comprising (I) a compound of formula (X) and (II) one or more agents selected, independently of each other, from any one of (A) to (G): (A) a certain fungicide; (B) a certain insecticide or nematicide; (C) a certain protein produced by the plant pathogenic bacterium, Erwinia amylovora; (D) a certain biological strain, (E) a certain Isoflavone; (F) a plant growth regulator; and (G) a plant activator, such as acibenzolar-S-methyl, wherein compound of formula (X) is a mixture of (formulas)

If you are interested in 153719-23-4, you can contact me at any time and look forward to more communication.Synthetic Route of 153719-23-4

Reference£º
Thiazole | C3H8994NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Article£¬once mentioned of 153719-23-4, Application In Synthesis of N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

Neonicotinoid insecticides are a group of plant protectants frequently detected in surface waters at low concentrations. Aquatic invertebrates therefore have the potential to be exposed chronically to low concentrations of neonicotinoids. The cladocerans Daphnia magna and Ceriodaphnia dubia are among the most commonly used invertebrate test species in aquatic toxicology. Both species are known to be acutely insensitive to neonicotinoids, and while chronic toxicity has been characterized for D. magna, little research has been conducted with C. dubia. In the present study we conducted 7-d static-renewal life cycle tests for 6 neonicotinoids (acetamiprid, clothianidin, dinotefuran, imidacloprid, thiacloprid, and thiamethoxam) with C. dubia, and a 21-d test with imidacloprid with D. magna. 7-d LC50s for C. dubia ranged from 8.42 mg L?1 for imidacloprid to > 100 mg L?1 for clothianidin; 7-d reproduction EC50s were 2.98 for thiacloprid, to > 67 mg L?1 for dinotefuran. D. magna were less sensitive than C. dubia to imidacloprid, by 4-fold for lethality and 1.5-fold for reproduction; however, acute-to-chronic ratios (ACRs) were similar. ACRs, based on 48-h acute LC50s and 7- or 21-d chronic reproduction EC10s, ranged from 5.4 for acetamiprid to 53.0 for imidacloprid (mean 36.6, CV = 51%). Chronic toxicity values for both species were orders of magnitude greater than concentrations reported in the environment, and thus hazard to these cladocerans is negligible.

Neonicotinoid insecticides are a group of plant protectants frequently detected in surface waters at low concentrations. Aquatic invertebrates therefore have the potential to be exposed chronically to low concentrations of neonicotinoids. The cladocerans Daphnia magna and Ceriodaphnia dubia are among the most commonly used invertebrate test species in aquatic toxicology. Both species are known to be acutely insensitive to neonicotinoids, and while chronic toxicity has been characterized for D. magna, little research has been conducted with C. dubia. In the present study we conducted 7-d static-renewal life cycle tests for 6 neonicotinoids (acetamiprid, clothianidin, dinotefuran, imidacloprid, thiacloprid, and thiamethoxam) with C. dubia, and a 21-d test with imidacloprid with D. magna. 7-d LC50s for C. dubia ranged from 8.42 mg L?1 for imidacloprid to > 100 mg L?1 for clothianidin; 7-d reproduction EC50s were 2.98 for thiacloprid, to > 67 mg L?1 for dinotefuran. D. magna were less sensitive than C. dubia to imidacloprid, by 4-fold for lethality and 1.5-fold for reproduction; however, acute-to-chronic ratios (ACRs) were similar. ACRs, based on 48-h acute LC50s and 7- or 21-d chronic reproduction EC10s, ranged from 5.4 for acetamiprid to 53.0 for imidacloprid (mean 36.6, CV = 51%). Chronic toxicity values for both species were orders of magnitude greater than concentrations reported in the environment, and thus hazard to these cladocerans is negligible.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application In Synthesis of N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide. In my other articles, you can also check out more blogs about 153719-23-4

Reference£º
Thiazole | C3H8898NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Article£¬once mentioned of 153719-23-4, HPLC of Formula: C8H10ClN5O3S

Bradysia odoriphaga Yang et Zhang is a destructive insect pest of Chinese chives. To understand the current status of insecticide resistance of B. odoriphaga in China, the sensitivity variation of eight field populations to six commonly used insecticides, including chlorpyrifos, phoxim, imidacloprid, thiamethoxam, clothianidin and beta-cypermethrin were evaluated. The results showed that almost all the tested B. odoriphaga populations had developed moderate to high resistance to chlorpyrifos and phoxim. There were different resistance levels found in the eight field populations among the three neonicotinoids, imidacloprid, thiamethoxam and clothianidin. Imidacloprid was very effective against B. odoriphaga in most tested populations except those from Yangzhou (10.35-fold) and Tangshan (14.56-fold). While four populations kept susceptible to thiamethoxam, the other four populations showed decreased susceptibility or low resistance. To clothianidin, five populations displayed moderate resistance, two populations displayed low resistance, and one population exhibited susceptibility, respectively. All the tested populations were resistance to beta-cypermethrin, the highest resistance was found in the Tangshan population with a resistance ratio of 172.56-fold. The results of this study provided valuable information for choosing insecticides for control and integrated resistance management of B. odoriphaga.

Bradysia odoriphaga Yang et Zhang is a destructive insect pest of Chinese chives. To understand the current status of insecticide resistance of B. odoriphaga in China, the sensitivity variation of eight field populations to six commonly used insecticides, including chlorpyrifos, phoxim, imidacloprid, thiamethoxam, clothianidin and beta-cypermethrin were evaluated. The results showed that almost all the tested B. odoriphaga populations had developed moderate to high resistance to chlorpyrifos and phoxim. There were different resistance levels found in the eight field populations among the three neonicotinoids, imidacloprid, thiamethoxam and clothianidin. Imidacloprid was very effective against B. odoriphaga in most tested populations except those from Yangzhou (10.35-fold) and Tangshan (14.56-fold). While four populations kept susceptible to thiamethoxam, the other four populations showed decreased susceptibility or low resistance. To clothianidin, five populations displayed moderate resistance, two populations displayed low resistance, and one population exhibited susceptibility, respectively. All the tested populations were resistance to beta-cypermethrin, the highest resistance was found in the Tangshan population with a resistance ratio of 172.56-fold. The results of this study provided valuable information for choosing insecticides for control and integrated resistance management of B. odoriphaga.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.HPLC of Formula: C8H10ClN5O3S, you can also check out more blogs about153719-23-4

Reference£º
Thiazole | C3H8936NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Patent£¬once mentioned of 153719-23-4, COA of Formula: C8H10ClN5O3S

At least one kind of compound selected from a salt of 1 [to] 2 – amino nicotine acid ester derivative ¡¤ sterilization by enhancing insecticidal activity, a variety of harmful organisms exhibiting a pest control agent composition for controlling effect at low doses. [Solution] Type I:(In the formula, R1 C represents a hydrogen atom or1 – C4 The alkyl, R2 Represents a hydrogen atom, a halogen atom, C1 – C4 C alkyl group or1 – C4 The alkoxy group, a nitrogen atom or a methine group (CH) represents A, Y is an oxygen atom, a methylene group (CH2 ) Or groups methylenoxy (OCH2 ) Showing) and at least 1 species selected from 2 – amino nicotine acid ester derivative represented by the compound, at least one kind of compound selected from a compound having insecticidal activity 1 mixing. [Drawing] no (by machine translation)

At least one kind of compound selected from a salt of 1 [to] 2 – amino nicotine acid ester derivative ¡¤ sterilization by enhancing insecticidal activity, a variety of harmful organisms exhibiting a pest control agent composition for controlling effect at low doses. [Solution] Type I:(In the formula, R1 C represents a hydrogen atom or1 – C4 The alkyl, R2 Represents a hydrogen atom, a halogen atom, C1 – C4 C alkyl group or1 – C4 The alkoxy group, a nitrogen atom or a methine group (CH) represents A, Y is an oxygen atom, a methylene group (CH2 ) Or groups methylenoxy (OCH2 ) Showing) and at least 1 species selected from 2 – amino nicotine acid ester derivative represented by the compound, at least one kind of compound selected from a compound having insecticidal activity 1 mixing. [Drawing] no (by machine translation)

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.COA of Formula: C8H10ClN5O3S, you can also check out more blogs about153719-23-4

Reference£º
Thiazole | C3H8940NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Article£¬once mentioned of 153719-23-4, Quality Control of: N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

Ionic liquids may be considered as “environment-friendly solvents” for sparingly soluble pesticides. In this study, a series of aqueous ionic liquids (ILs) with different cations and different anions was used as environment-friendly alternative to harmful organic solvents sparingly dissolved in soluble pesticides (metolachlor, acetochlor, clethodim, thiamethoxam, and prochloraz). The aggregation behavior of aqueous ILs was investigated through surface tension measurement. Minimum area per IL molecule (Amin) values from the surface tension measurement showed that alkyl chain length and the halide anions strongly affect the aggregation behavior of ILs and the solubilization of pesticides. The solubility of metolachlor, acetochlor, clethodim, thiamethoxam, nitenpyram, and prochloraz in aqueous ILs increased. More importantly, the solubility of prochloraz in [C10mim][I] became 5771-fold higher than that in pure water. The substantially enhanced solubility of the above pesticides proved that aqueous ILs are promising environment-friendly solvents for pesticides that are commercially processed in emulsifiable concentrate (EC) formulation.

Ionic liquids may be considered as “environment-friendly solvents” for sparingly soluble pesticides. In this study, a series of aqueous ionic liquids (ILs) with different cations and different anions was used as environment-friendly alternative to harmful organic solvents sparingly dissolved in soluble pesticides (metolachlor, acetochlor, clethodim, thiamethoxam, and prochloraz). The aggregation behavior of aqueous ILs was investigated through surface tension measurement. Minimum area per IL molecule (Amin) values from the surface tension measurement showed that alkyl chain length and the halide anions strongly affect the aggregation behavior of ILs and the solubilization of pesticides. The solubility of metolachlor, acetochlor, clethodim, thiamethoxam, nitenpyram, and prochloraz in aqueous ILs increased. More importantly, the solubility of prochloraz in [C10mim][I] became 5771-fold higher than that in pure water. The substantially enhanced solubility of the above pesticides proved that aqueous ILs are promising environment-friendly solvents for pesticides that are commercially processed in emulsifiable concentrate (EC) formulation.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Quality Control of: N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, you can also check out more blogs about153719-23-4

Reference£º
Thiazole | C3H8908NS – PubChem,
Thiazole | chemical compound | Britannica

153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 153719-23-4, HPLC of Formula: C8H10ClN5O3S

The invention belongs to the field of agricultural chemicals, relates to a containing two active component synergistic compound composition. Containing A, B two kinds of active constituent, component selected from pyrimidine manman amine A, component B selected from nicotinamide or insect growth regulator such as insecticide, acaricide; component A, B two active component weight ratio of 1:99 to 99:1; wherein pyrimidine manman amine structural formula as follows, the composition of the invention has obvious synergistic action, can be used for controlling various pests, mites. (by machine translation)

The invention belongs to the field of agricultural chemicals, relates to a containing two active component synergistic compound composition. Containing A, B two kinds of active constituent, component selected from pyrimidine manman amine A, component B selected from nicotinamide or insect growth regulator such as insecticide, acaricide; component A, B two active component weight ratio of 1:99 to 99:1; wherein pyrimidine manman amine structural formula as follows, the composition of the invention has obvious synergistic action, can be used for controlling various pests, mites. (by machine translation)

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.HPLC of Formula: C8H10ClN5O3S. In my other articles, you can also check out more blogs about 153719-23-4

Reference£º
Thiazole | C3H8872NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Patent£¬once mentioned of 153719-23-4, Product Details of 153719-23-4

The invention discloses a seed treatment composition and its application, relates to the technical field of the pesticide. The invention of the seed treatment composition containing the active ingredient A and effective ingredient B. Wherein A is […], Fludioxonil B is, the effective ingredient B A with the weight ratio of 1 – 50:1 – 30. The seed treatment composition can be from different target spot carries on the effects, as seed provide all-round protection, its good environmental compatibility, low toxicity, and animals, natural enemies and other biological safety, which belongs to the broad-spectrum of the seed treatment composition. Has higher synergistic effect, and to reduce the cost, the control effect is obviously superior to single agents. The broad-spectrum of the seed treatment composition, it has obvious promotional value. (by machine translation)

The invention discloses a seed treatment composition and its application, relates to the technical field of the pesticide. The invention of the seed treatment composition containing the active ingredient A and effective ingredient B. Wherein A is […], Fludioxonil B is, the effective ingredient B A with the weight ratio of 1 – 50:1 – 30. The seed treatment composition can be from different target spot carries on the effects, as seed provide all-round protection, its good environmental compatibility, low toxicity, and animals, natural enemies and other biological safety, which belongs to the broad-spectrum of the seed treatment composition. Has higher synergistic effect, and to reduce the cost, the control effect is obviously superior to single agents. The broad-spectrum of the seed treatment composition, it has obvious promotional value. (by machine translation)

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Product Details of 153719-23-4. In my other articles, you can also check out more blogs about 153719-23-4

Reference£º
Thiazole | C3H8840NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Patent£¬once mentioned of 153719-23-4, Product Details of 153719-23-4

The invention relates to a triazole and nicotine compound seed treating agent and a preparation method thereof. The effective component is a mixture of triazole bactericide and nicotine insecticide in a mass ratio of 1: (0.5-5), the triazole bactericide is tetraconazole, and the nicotine insecticide is thiamethoxam or clothianidin. The treating agent can be prepared into dispersable seed treating granule or suspending agent or seed coating agent. Compared with single preparations, the bactericidal effect of the composition tetraconazole is obviously improved, which proves that the effect of single pesticide is better due to the mixing of the triazole and nicotine, the prevention and control effect and scope are improved; the prevention and cure range of the compound is enlarged and the effect of killing both aphid and bacteria is realized, as compared with the single preparations in markets.

The invention relates to a triazole and nicotine compound seed treating agent and a preparation method thereof. The effective component is a mixture of triazole bactericide and nicotine insecticide in a mass ratio of 1: (0.5-5), the triazole bactericide is tetraconazole, and the nicotine insecticide is thiamethoxam or clothianidin. The treating agent can be prepared into dispersable seed treating granule or suspending agent or seed coating agent. Compared with single preparations, the bactericidal effect of the composition tetraconazole is obviously improved, which proves that the effect of single pesticide is better due to the mixing of the triazole and nicotine, the prevention and control effect and scope are improved; the prevention and cure range of the compound is enlarged and the effect of killing both aphid and bacteria is realized, as compared with the single preparations in markets.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Product Details of 153719-23-4. In my other articles, you can also check out more blogs about 153719-23-4

Reference£º
Thiazole | C3H8796NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, molecular formula is C8H10ClN5O3S. In a Patent£¬once mentioned of 153719-23-4, Safety of N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

The invention provides a fenoxycarb insecticidal composition, which comprises fenoxycarb and a second insecticidal ingredient; wherein the weight ratio of fenoxycarb to second insecticidal ingredient is 80: 1-1: 80, and the second insecticidal ingredient is preferably thiamethoxam, or emamectin benzoate, or a combination of thiamethoxam and emamectin benzoate. The provided fenoxycarb insecticidal composition has the advantages that the synergy effect is obvious, LC50 can be obviously reduced, pesticide amount is reduced, and the insecticidal composition has characteristics of wide insecticidal spectrum, high efficiency, low toxicity, low prevention and treatment cost.

The invention provides a fenoxycarb insecticidal composition, which comprises fenoxycarb and a second insecticidal ingredient; wherein the weight ratio of fenoxycarb to second insecticidal ingredient is 80: 1-1: 80, and the second insecticidal ingredient is preferably thiamethoxam, or emamectin benzoate, or a combination of thiamethoxam and emamectin benzoate. The provided fenoxycarb insecticidal composition has the advantages that the synergy effect is obvious, LC50 can be obviously reduced, pesticide amount is reduced, and the insecticidal composition has characteristics of wide insecticidal spectrum, high efficiency, low toxicity, low prevention and treatment cost.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 153719-23-4 is helpful to your research., Safety of N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

Reference£º
Thiazole | C3H8825NS – PubChem,
Thiazole | chemical compound | Britannica