Tag: M.W:200-300

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. 80945-86-4, C7H3BrClNS. A document type is Patent, introducing its new discovery., Formula: C7H3BrClNS

The invention relates to a 2-(3-cyano-4-alkoxy) phenyl-4-substituted thiazole-5-formic acid compound which has xanthine oxidase inhibitory activity and is shown in a general formula I, a composition and preparation methods thereof. The invention also relates to applications of the compound and the composition thereof to preparation of medicaments for treating and/or preventing hyperuricemia and gout diseases. In the formula I, R2 is substituted or unsubstituted phenyl or a substituted or unsubstituted heteroaromatic radical, R1 is a substitutive aliphatic group of a straight chain or a branched chain, substituted or unsubstituted alicyclic hydrocarbonyl or substituted or unsubstituted aryl alkyl and A is an oxygen atom, a sulfur atom or a nitrogen atom.

Interested yet? Keep reading other articles of 80945-86-4!, Formula: C7H3BrClNS

Reference£º
Thiazole | C3H10888NS – 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.5331-91-9, Name is 5-Chlorobenzo[d]thiazole-2(3H)-thione, molecular formula is C7H4ClNS2. In a Patent£¬once mentioned of 5331-91-9, Product Details of 5331-91-9

Novel 2-substituted-3-hydroxythiazolo[2,3-b]benzo-(and azabenzo)thiazolium salts, the mesoionic didehydro derivatives thereof and related compounds are disclosed, as well as the use thereof as modulators of the immune response.

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.Product Details of 5331-91-9, you can also check out more blogs about5331-91-9

Reference£º
Thiazole | C3H6313NS – PubChem,
Thiazole | chemical compound | Britannica

16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 16112-21-3, HPLC of Formula: C14H11NS

Flexible di/trimeric substituted imidazolium salts are prepared under conventional/solvent free silica supported approaches. Solid supported approaches are superior than the conventional method like environment friendly, higher yield, shorter reaction time and easy workup procedure. We have studied the catalytic activities of our synthesized di/trimeric imidazolium salts for one-pot preparation of benzoxazole derivatives under conventional/Muffle furnace conditions. We have monitored the efficiency of recycled flexible di/trimeric imidazolium salts up to fourth cycles showed excellent responses. We have studied the MIC and MBC of our di/trimeric imidazolium salts against Gram positive/negative microorganisms under micro dilution method. Nitro substituted imidazolium salts showed excellent screening responses than the unsubstituted compounds. Computer assisted docking analysis is carried out for all our synthesized compounds. The host-guest interaction via hydrogen bonding between standard and our drug molecules against various human Gram positive and negative pathogens are compared. From the docking analysis, our drug molecules showed effective interaction against test pathogens.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.HPLC of Formula: C14H11NS. In my other articles, you can also check out more blogs about 16112-21-3

Reference£º
Thiazole | C3H733NS – 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. 86978-24-7, Name is (Z)-2-(2-((tert-Butoxycarbonyl)amino)thiazol-4-yl)pent-2-enoic acid, molecular formula is C13H18N2O4S. In a Article£¬once mentioned of 86978-24-7, category: thiazole

A stereoselective or exclusive approach to a series of ethyl (Z)-2-(2-substituted-thiazol-4-yl)pent-2-enoates from ethyl (E/Z)-2-(2- bromoacetyl)pent-2-enoate and thioureas or thioamides was reported in good yields. This approach involves a quaternary carbon stereocontrolled cis-configuration formation, and opportunely blocking a potential E/Z isomerization. The practical applicability was highlighted by the synthesis of (Z)-2-(2-tert-butoxycarbonylaminothiazol-4-yl)pent-2-enoic acid, a commercially important side-chain material of cefcapene pivoxil, in a two-step procedure. Georg Thieme Verlag Stuttgart ¡¤ New York.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.category: thiazole. In my other articles, you can also check out more blogs about 86978-24-7

Reference£º
Thiazole | C3H109NS – PubChem,
Thiazole | chemical compound | Britannica

5331-91-9, Name is 5-Chlorobenzo[d]thiazole-2(3H)-thione, molecular formula is C7H4ClNS2, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 5331-91-9, Recommanded Product: 5-Chlorobenzo[d]thiazole-2(3H)-thione

A compound of formula (I), or a pharmaceutically acceptable salt thereof: STR1 wherein X is halogen, trifluoromethyl, cyano, C 1-6 -alkoxy, C 1-6 -alkylthio, C 1-6 -alkylamino or C 1-6 -dialkylamino;R 1 and R 4 are H or straight or branched C 1-6 -alkyl or trifluoromethyl or R 1 and R 4 together form a cycloalkyl ring;Y is O, S, SO 2, NH or N-alkyl;R 5 is selected from optionally substituted heterocycles.R 6 and R 7 are hydrogen, benzoyl or C 1-6 -alkanoyl.The compounds have been found useful for treating central nervous system and cardiovascular ailments.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 5-Chlorobenzo[d]thiazole-2(3H)-thione. In my other articles, you can also check out more blogs about 5331-91-9

Reference£º
Thiazole | C3H6378NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 777-12-8, Name is 6-(Trifluoromethyl)benzo[d]thiazol-2-amine,molecular formula is C8H5F3N2S, is a conventional compound. this article was the specific content is as follows.Recommanded Product: 6-(Trifluoromethyl)benzo[d]thiazol-2-amine

The S -benzyl thioester and methyl ester derivatives of a representative 4-pyridinone-based carboxylic acid were sufficiently activated to react efficiently in amide coupling reactions with the amide anion generated in situ from the N -trimethylsilyl derivative of different weakly nucleophilic heteroarylamines. In acetonitrile as solvent, the precipitated diheteroarylamide products were isolated in pure form by vacuum filtration. This simple amide bond forming protocol can be readily adapted to the parallel synthesis of compound libraries.

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Reference£º
Thiazole | C3H6685NS – 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 present invention relates to pesticides which contains the thiamethoxam […] synergistic composition of the humic acid, effective constituent of the thiamethoxam, fipronil and humic acid composition, the thiamethoxam the weight percentage of the composition is 0.5% – 2.0%, fipronil and the weight percentage of the composition is 0.5-3.0%, in the composition of the humic acid the weight percentage of 1.0% – 5.0%. This invention, through thiamethoxam, fipronil, humic acid compounding for granular pesticide of preventing the peanut white, can greatly improve the potency, pesticide is reduced, the use cost is reduced, prolonging the duration of the effect, at the same time be able to overcome the shortcoming of the single resistance is easily generated. (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 | C3H8702NS – PubChem,
Thiazole | chemical compound | Britannica

Electric Literature of 2941-48-2. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 2941-48-2, Name is 2,5-Dichlorobenzothiazole

A compound of formula (I): STR1 in which X, n, B and Y are as defined in the description. useful as cytokine inhibitors.

If you are hungry for even more, make sure to check my other article about 2941-48-2. Electric Literature of 2941-48-2

Reference£º
Thiazole | C3H1733NS – PubChem,
Thiazole | chemical compound | Britannica

Electric Literature of 16112-21-3. Let¡¯s face it, organic chemistry can seem difficult to learn. Especially from a beginner¡¯s point of view. Like 16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole. In a document type is Patent, introducing its new discovery.

The present invention provides a green synthetic 2 the thiazole derivatives substituted benzo […] method, the method comprises: in CO 2 presence, the invention uses water as a solvent, an aldehyde, ortho-amino aromatic disulfide and metal sulfide contact, to obtain the the 2 […] substituted benzo thiazole derivatives. Compared with the prior art, the invention utilizes the aromatic ortho-amino disulphides and more aldehydes in water and CO 2 react under the action of, the fast and efficient synthesis 2 the thiazole derivatives substituted benzo […], the used raw material is stable and easy to obtain, the cost is low, synthetic method is easy and simple to handle, the step is short, high yield, the product is easy to be purified, is friendly to the environment, and the like. (by machine translation)

If you are interested in 16112-21-3, you can contact me at any time and look forward to more communication.Electric Literature of 16112-21-3

Reference£º
Thiazole | C3H635NS – 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 16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, Product Details of 16112-21-3.

Ni-based catalytic systems for the arylation of heteroarenes with aryl halides and triflates have been established. Ni(OAc)2/bipy is a general catalyst for aryl bromides/iodides, and Ni(OAc)2/dppf is effective for aryl chlorides/triflates. Thiazole, benzothiazole, oxazole, benzoxazole, and benzimidazole are applicable as heteroarene coupling partners. A rapid synthesis of febuxostat, a drug for gout and hyperuricemia, is also demonstrated.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Product Details of 16112-21-3. In my other articles, you can also check out more blogs about 16112-21-3

Reference£º
Thiazole | C3H695NS – PubChem,
Thiazole | chemical compound | Britannica