Category: 153719-23-4

In an article, published in an article, once mentioned the application of 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, is a conventional compound. this article was the specific content is as follows.Safety of N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

The present invention relates to a method to overcome negative effects of the treatment of seeds with insecticides, acaricides or nematicides on the germination of seeds and vitality of seedlings. The inventive method markedly enhances germination and vitality of seeds that are treated with insecticides, acaricides or nematicides. The present invention describes a method that at least comprises the following steps: 1) Hydration of the seed 2) Followed by drying of the seed 3) Followed by a treatment of the seed with insecticidal, acaricidal, or nematicidal compounds.

The present invention relates to a method to overcome negative effects of the treatment of seeds with insecticides, acaricides or nematicides on the germination of seeds and vitality of seedlings. The inventive method markedly enhances germination and vitality of seeds that are treated with insecticides, acaricides or nematicides. The present invention describes a method that at least comprises the following steps: 1) Hydration of the seed 2) Followed by drying of the seed 3) Followed by a treatment of the seed with insecticidal, acaricidal, or nematicidal compounds.

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Reference£º
Thiazole | C3H8739NS – PubChem,
Thiazole | chemical compound | Britannica

Reference of 153719-23-4, Chemistry can be defined as the study of matter and the changes it undergoes. You¡¯ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology.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, introducing its new discovery.

The invention discloses a containing two halogenating pyrazole amide with the insecticidal composition of the thiamethoxam, including 1st active ingredient b halogenating pyrazole amide and 2nd active ingredient thiamethoxam and commonly used auxiliary component, two thiamethoxam halogenating pyrazole amide and the weight ratio of 10:1 – 1:4. By the indoor and outdoor test shows, the present invention insecticidal composition has an obvious role in synergism, the crops on a plurality of pest control effect is obviously superior to the single use alone. At the same time reducing the use of pesticides, reduces the pesticide in the residue on the crops, thereby reducing the pollution of the environment, delays the generation of drug resistance. (by machine translation)

The invention discloses a containing two halogenating pyrazole amide with the insecticidal composition of the thiamethoxam, including 1st active ingredient b halogenating pyrazole amide and 2nd active ingredient thiamethoxam and commonly used auxiliary component, two thiamethoxam halogenating pyrazole amide and the weight ratio of 10:1 – 1:4. By the indoor and outdoor test shows, the present invention insecticidal composition has an obvious role in synergism, the crops on a plurality of pest control effect is obviously superior to the single use alone. At the same time reducing the use of pesticides, reduces the pesticide in the residue on the crops, thereby reducing the pollution of the environment, delays the generation of drug resistance. (by machine translation)

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Reference£º
Thiazole | C3H8859NS – PubChem,
Thiazole | chemical compound | Britannica

Electric Literature 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 an insecticidal composition for killing […], compounds containing synergistic active component as follows: component selected from A […], component B mitochondrial respiratory inhibit agent selected from such insecticidal acaricides, growth inhibiting agent type of insecticidal acaricide, miticide killing neurotoxin, pyrethroid insecticide acaricide, miticide pesticidal macrolides, carbamates insectcidal acaricide, and the like. Insecticidal, acaricidal composition of the present invention is especially suitable for the fruit to the, cotton, vegetables and ornamental plant the phytophagous mites. (by machine translation)

The invention discloses an insecticidal composition for killing […], compounds containing synergistic active component as follows: component selected from A […], component B mitochondrial respiratory inhibit agent selected from such insecticidal acaricides, growth inhibiting agent type of insecticidal acaricide, miticide killing neurotoxin, pyrethroid insecticide acaricide, miticide pesticidal macrolides, carbamates insectcidal acaricide, and the like. Insecticidal, acaricidal composition of the present invention is especially suitable for the fruit to the, cotton, vegetables and ornamental plant the phytophagous mites. (by machine translation)

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Reference£º
Thiazole | C3H8830NS – 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, Quality Control of: N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

The total synthesis of (+)-crocacin D has been achieved in 15 steps (9 isolated intermediates) and 14% overall yield from commercially available starting materials and using (+)-crocacin C as a key intermediate. A number of simplified analogues and their biological activities are also reported.

The total synthesis of (+)-crocacin D has been achieved in 15 steps (9 isolated intermediates) and 14% overall yield from commercially available starting materials and using (+)-crocacin C as a key intermediate. A number of simplified analogues and their biological activities are also reported.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Quality Control 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 | C3H8689NS – PubChem,
Thiazole | chemical compound | Britannica

Electric Literature 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 relates to pesticidal mixtures comprising as active compounds 1) at least one cyanosulfoximine compound I of the formula (I) wherein R1, R2 and G are defined in the description; and 2) at least one active compound II selected from a group A comprising acteylcholine esterase inhibitors, GABA-gated chloride channel antagonists, sodium channel modulators, nicotinic acetylcholine receptor agonists/antagonists, chloride channel activators, juvenile hormone mimics, compounds affecting the oxidative phosphorylation, inhibitors of the chitin biosynthesis, moulting disruptors, inhibitors of the MET, voltage-dependent sodium channel blockers, inhibitors of the lipid synthesis and other compounds as defined in the description, in synergistically effective amounts. The invention relates further to methods and use of these mixtures for combating insects, arachnids or nematodes in and on plants, and for protecting such plants being infested with pests and also for protecting seeds.

The invention relates to pesticidal mixtures comprising as active compounds 1) at least one cyanosulfoximine compound I of the formula (I) wherein R1, R2 and G are defined in the description; and 2) at least one active compound II selected from a group A comprising acteylcholine esterase inhibitors, GABA-gated chloride channel antagonists, sodium channel modulators, nicotinic acetylcholine receptor agonists/antagonists, chloride channel activators, juvenile hormone mimics, compounds affecting the oxidative phosphorylation, inhibitors of the chitin biosynthesis, moulting disruptors, inhibitors of the MET, voltage-dependent sodium channel blockers, inhibitors of the lipid synthesis and other compounds as defined in the description, in synergistically effective amounts. The invention relates further to methods and use of these mixtures for combating insects, arachnids or nematodes in and on plants, and for protecting such plants being infested with pests and also for protecting seeds.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 153719-23-4, help many people in the next few years., Electric Literature of 153719-23-4

Reference£º
Thiazole | C3H8790NS – PubChem,
Thiazole | chemical compound | Britannica

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 153719-23-4, Name is N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide, Recommanded Product: 153719-23-4.

The invention discloses a containing tetrazole amide and neonicotinoid insecticide composition, this composition is characterized in that: comprising an active ingredient A, active ingredient B. Wherein the active ingredient A is tetrazole amide, active ingredient is thiamethoxam B, Imidacloprid, acetamiprid, pymetrozine, dinotefuran, clothianidine in any of a, and the active ingredient A and active ingredient B in a weight ratio of 1:80 – 80:1, composition made wettable powder, water dispersible granule, a suspending agent, suspension emulsion, aqueous emulsion, micro-emulsion. The compositions of the invention can be used for preventing a plurality of pests on the crops, and has obvious synergistic action, and has reduced the pesticide dosage, safe to people and animals, without damage, and good environmental compatibility; preparation improved adhesion, erosion-resistant. (by machine translation)

The invention discloses a containing tetrazole amide and neonicotinoid insecticide composition, this composition is characterized in that: comprising an active ingredient A, active ingredient B. Wherein the active ingredient A is tetrazole amide, active ingredient is thiamethoxam B, Imidacloprid, acetamiprid, pymetrozine, dinotefuran, clothianidine in any of a, and the active ingredient A and active ingredient B in a weight ratio of 1:80 – 80:1, composition made wettable powder, water dispersible granule, a suspending agent, suspension emulsion, aqueous emulsion, micro-emulsion. The compositions of the invention can be used for preventing a plurality of pests on the crops, and has obvious synergistic action, and has reduced the pesticide dosage, safe to people and animals, without damage, and good environmental compatibility; preparation improved adhesion, erosion-resistant. (by machine translation)

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

Reference£º
Thiazole | C3H8861NS – 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, Quality Control of: N-(3-((2-Chlorothiazol-5-yl)methyl)-5-methyl-1,3,5-oxadiazinan-4-ylidene)nitramide

The invention provides a of thiamethoxam and azoxystrobin pesticide composition, wherein the thiamethoxam content is 1 – 85%, azoxystrobin content is 1 – 85%. The invention two kinds of pesticide composition can effectively control the various aphid, leafhopper, plant hopper class, Dialeurodes, beetle larvae, potato beetles, nematode, ground beetle, the pests such as leaf, at the same time to powdery mildew, rust, ying dry sickness, blotch, downy mildew, rice blast or the like have good activity, can be used for stem leaf atomization, seed treatment, can also soil treatment. (by machine translation)

The invention provides a of thiamethoxam and azoxystrobin pesticide composition, wherein the thiamethoxam content is 1 – 85%, azoxystrobin content is 1 – 85%. The invention two kinds of pesticide composition can effectively control the various aphid, leafhopper, plant hopper class, Dialeurodes, beetle larvae, potato beetles, nematode, ground beetle, the pests such as leaf, at the same time to powdery mildew, rust, ying dry sickness, blotch, downy mildew, rice blast or the like have good activity, can be used for stem leaf atomization, seed treatment, can also soil treatment. (by machine translation)

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Quality Control 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 | C3H8822NS – PubChem,
Thiazole | chemical compound | Britannica

Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn¡¯t involve a screen. 153719-23-4, C8H10ClN5O3S. A document type is Patent, introducing its new discovery., Formula: C8H10ClN5O3S

The present invention relates to novel active compound combinations comprising of at least two fungicidal components A and B and at least one insecticidal component C. A, B and C may be selected from the following compounds: A) the compounds of the general formula (I) in which the radicals R1 and R2 have the meanings given in the description, B) an acylalanine of the general formula (II) in which R3 represents benzyl, furyl or methoxymethyl and * represents a carbon in the R- or S-configuration, the S-configuration being preferred, or fludioxonil or azoxystrobin C) a chloronicotinyl of the general formula (III) where the radicals Het, R, X and A have the meanings given in the description, or rynaxapyr, fipronil, tefluthrin. The active compound combinations are highly suitable for controlling unwanted phytopathogenic fungi and for controlling animal pests. The active compound combinations according to the invention are particularly suitable for treating seed.

The present invention relates to novel active compound combinations comprising of at least two fungicidal components A and B and at least one insecticidal component C. A, B and C may be selected from the following compounds: A) the compounds of the general formula (I) in which the radicals R1 and R2 have the meanings given in the description, B) an acylalanine of the general formula (II) in which R3 represents benzyl, furyl or methoxymethyl and * represents a carbon in the R- or S-configuration, the S-configuration being preferred, or fludioxonil or azoxystrobin C) a chloronicotinyl of the general formula (III) where the radicals Het, R, X and A have the meanings given in the description, or rynaxapyr, fipronil, tefluthrin. The active compound combinations are highly suitable for controlling unwanted phytopathogenic fungi and for controlling animal pests. The active compound combinations according to the invention are particularly suitable for treating seed.

Interested yet? Keep reading other articles of 153719-23-4!, Formula: C8H10ClN5O3S

Reference£º
Thiazole | C3H8714NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route of 153719-23-4, Chemistry can be defined as the study of matter and the changes it undergoes. You¡¯ll sometimes hear it called the central science because it is the connection between physics and all the other sciences, starting with biology.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, introducing its new discovery.

A acetamiprid semi-antigen with the antigenic preparation method and application, characterized in that the antigen is composed of insect trunk states ding N – to a acetamiprid and amino butyric acid reaction; the states ding by insect trunk antigen is acetamiprid semi-antigen with a carrier protein obtained by coupling. The invention preparation of antigen presenting the specific acetamiprid antigenic determinant, such that the screen high specificity of monoclonal antibody acetamiprid become possible. Generating antibody of high specificity, high sensitivity, can be used for the establishment of the enzyme-linked immunosorbent assay method for rapidly measuring and colloidal gold, thereby realizing the tobacco and food ding rapid detection of insect trunk. (by machine translation)

A acetamiprid semi-antigen with the antigenic preparation method and application, characterized in that the antigen is composed of insect trunk states ding N – to a acetamiprid and amino butyric acid reaction; the states ding by insect trunk antigen is acetamiprid semi-antigen with a carrier protein obtained by coupling. The invention preparation of antigen presenting the specific acetamiprid antigenic determinant, such that the screen high specificity of monoclonal antibody acetamiprid become possible. Generating antibody of high specificity, high sensitivity, can be used for the establishment of the enzyme-linked immunosorbent assay method for rapidly measuring and colloidal gold, thereby realizing the tobacco and food ding rapid detection of insect trunk. (by machine translation)

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Reference£º
Thiazole | C3H8998NS – 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, Computed Properties of C8H10ClN5O3S

The insecticide thiamethoxam (TMX) is one of the most important neonicotinoid pesticides. The chromatographic methods currently employed to detect TMX require multiple operational steps. This study proposes a simple method that detects TMX via surface-enhanced Raman scattering (SERS) spectroscopy with Ag nanoparticles (NPs) as the SERS active substrate. Density functional theory (DFT) was used to calculate the structures and vibrational modes of the Ag? and Ag3?TMX complexes at the B3LYP/6-311++G(d,p)(C,H,N)/LanL2DZ(Ag) level of theory. The results reveal that the atoms in the thiazole ring all lie in the same plane, while the six-membered ring is perpendicular to the thiazole ring. Data from both Ultraviolet-visible and Raman spectroscopy indicated that TMX bonds to Ag through its nitro group, vertically. A weak intramolecular (N22?O23?H26) hydrogen bonding and Ag?O bands shift N?O symmetrical vibration to down to lower wavenumber. This was supported by the appearance of a strong 866 cm?1 band in the SERS spectrum assigned to the N?O symmetrical vibration coupled with the N?N stretching vibrational mode of different excitation wavelength. Notably, a good linear relationship was observed in the TMX concentration range 1.0 ¡Á 10?6?1.0 ¡Á 10?4mol¡¤L?1 (R2 = 0.9667). SERS is an extremely simple and rapid technique that requires little sample for analysis.

The insecticide thiamethoxam (TMX) is one of the most important neonicotinoid pesticides. The chromatographic methods currently employed to detect TMX require multiple operational steps. This study proposes a simple method that detects TMX via surface-enhanced Raman scattering (SERS) spectroscopy with Ag nanoparticles (NPs) as the SERS active substrate. Density functional theory (DFT) was used to calculate the structures and vibrational modes of the Ag? and Ag3?TMX complexes at the B3LYP/6-311++G(d,p)(C,H,N)/LanL2DZ(Ag) level of theory. The results reveal that the atoms in the thiazole ring all lie in the same plane, while the six-membered ring is perpendicular to the thiazole ring. Data from both Ultraviolet-visible and Raman spectroscopy indicated that TMX bonds to Ag through its nitro group, vertically. A weak intramolecular (N22?O23?H26) hydrogen bonding and Ag?O bands shift N?O symmetrical vibration to down to lower wavenumber. This was supported by the appearance of a strong 866 cm?1 band in the SERS spectrum assigned to the N?O symmetrical vibration coupled with the N?N stretching vibrational mode of different excitation wavelength. Notably, a good linear relationship was observed in the TMX concentration range 1.0 ¡Á 10?6?1.0 ¡Á 10?4mol¡¤L?1 (R2 = 0.9667). SERS is an extremely simple and rapid technique that requires little sample for analysis.

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

Reference£º
Thiazole | C3H8874NS – PubChem,
Thiazole | chemical compound | Britannica