Tag: M.W:200-300

40003-41-6, Name is 2-Bromo-4-methylthiazole-5-carboxylic acid, molecular formula is C5H4BrNO2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 40003-41-6, Application In Synthesis of 2-Bromo-4-methylthiazole-5-carboxylic acid

A series of thiazole derivatives which are substituted in the 2-position by a substituted morpholin-4-yl moiety, being selective inhibitors of PI3 kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions

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 2-Bromo-4-methylthiazole-5-carboxylic acid. In my other articles, you can also check out more blogs about 40003-41-6

Reference：
Thiazole | C3H2471NS – 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. 92-36-4, Name is 2-(4-Aminophenyl)-6-methylbenzothiazole, molecular formula is C14H12N2S. In a Article，once mentioned of 92-36-4, Recommanded Product: 92-36-4

A series of 17 compounds were synthesized based on the premise that the minimal pharmacophore for aldose reductase inhibition requires the presence of both an aryl group and polar group connected by a linking structure. Three groups of compounds were synthesized, the first possessing an aniline-4-(2?-6?-methylbenzothiazole) or 2-aminobenzothiazole group as the aryl group, the second possessing a 2-naphthyl as the aryl group and the third possessing either a 4-(2-phenylthiazole) or 2-(5-2?-nitrophenylfuran) as the aryl group. In all three of these groups the carboxylate or its methyl ester are linked to the aryl group through various lengths of methylene carbons and amide or cinnamide groups. Optimal activity was observed when the carboxylic group was separated from the aryl group by a linking structure of five atoms in length. Both a double bond and an amide moiety are well tolerated in the linking structure.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 92-36-4. In my other articles, you can also check out more blogs about 92-36-4

Reference：
Thiazole | C3H565NS – 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

A highly effective visible light-promoted “radical-type” coupling of N-heteroarenes with aryldiazonium salts in water has been developed. The reaction proceeds at room temperature with [Ru(bpy)3]Cl 2×6 H2O as a photosensitizer and a commercial household light bulb as a light source. Pyridine and a variety of substituted pyridines are effective substrates under these reaction conditions, and only monosubstituted products are formed with different regioselectivities. Using aqueous formic acid as solvent, an array of xanthenes, thiazole, pyrazine, and pyridazine are compatible with this new arylation approach. The broad substrate scope, mild reaction conditions, and use of water as reaction solvent make this procedure a practical and environmentally friendly method for the synthesis of compounds containing aryl-heteroaryl motifs. Cross-coupling reaction in water: An effective visible light promoted coupling of pyridine, substituted pyridines, xanthenes, thiazole, pyrazine, and pyridazine with aryldiazonium salts in water at room temperature has been developed (see scheme).

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：
Thiazole | C3H874NS – PubChem,
Thiazole | chemical compound | Britannica

Related Products of 29182-42-1. Let’s face it, organic chemistry can seem difficult to learn. Especially from a beginner’s point of view. Like 29182-42-1, Name is Ethyl 2-(benzo[d]thiazol-2-yl)acetate. In a document type is Article, introducing its new discovery.

Due to the similar structure and reactivity of cysteine (Cys), homocysteine (Hcy) and glutathione (GSH), the simultaneous discrimination of Cys over Hcy and GSH by a single fluorescent sensor is still a great challenge. In this work, a benzothiazole-pyimidine-based boron difluoride complex (BPB) was developed as a new fluorescent sensor for Cys. The sensor exhibits a highly selective “turn-on” response to cysteine over Hcy, GSH and other amino acids in aqueous solution at physiological pH. The observed pseudo-first-order rate constant for the reaction of BPB with Cys was calculated to be about 0.062min-1. The detection limit of this sensor for Cys was determined to be 332nm, and bioimaging of exogenous Cys by this sensor was successfully applied in living cells, thus indicating that this sensor holds great potential for biological applications. A not so typical response: A fluorescent Cys sensor that featured a highly selective “turn-on” response to cysteine over Hcy, GSH, and other amino acids was developed.

If you are interested in 29182-42-1, you can contact me at any time and look forward to more communication.Related Products of 29182-42-1

Reference：
Thiazole | C3H7857NS – 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 768-11-6, Name is 5-Bromobenzothiazole, name: 5-Bromobenzothiazole.

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions associated with the enzyme glucosylceramide synthase (GCS).

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.name: 5-Bromobenzothiazole. In my other articles, you can also check out more blogs about 768-11-6

Reference：
Thiazole | C3H6137NS – 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.4175-77-3, Name is 2,4-Dibromothiazole, molecular formula is C3HBr2NS. In a Patent，once mentioned of 4175-77-3, COA of Formula: C3HBr2NS

The present invention relates to novel Heterocycle-Substituted Tetracyclic Compounds of Formula (I): (I) and pharmaceutically acceptable salts thereof, wherein A, A’, R 2 R 3, R 4 and R are as defined herein. The present invention also relates to compositions comprising at least one Heterocycle-Substituted Tetracyclic Compound, and methods of using the Heterocycle-Substituted Tetracyclic Compounds for treating or preventing HCV infection in a patient.

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 4175-77-3 is helpful to your research., COA of Formula: C3HBr2NS

Reference：
Thiazole | C3H1272NS – PubChem,
Thiazole | chemical compound | Britannica

Related Products of 5331-91-9, An article , which mentions 5331-91-9, molecular formula is C7H4ClNS2. The compound – 5-Chlorobenzo[d]thiazole-2(3H)-thione played an important role in people’s production and life.

Seven novel 3-(1-(2-(2,7a-dihydrobenzo[d]thiazol-2-ylthio)acetyl)-5- substituted-phenyl-4,5-dihydro-1H-pyrazol-3-yl)-2H-chromen-2-one derivatives were synthesized and characterized by 1H NMR and 13 C NMR. All of the compounds have been screened for their anticancer activity. The bioassay tests show that compound 4g exhibited potentially high activity against human gastric cancer cell SGC-7901 with IC50 value of 6.99±1.10 mug/mL. Docking simulation was performed to position compound 4g into the telomerase (3DU6) active site to determine the probable binding model.

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 5331-91-9, help many people in the next few years., Related Products of 5331-91-9

Reference：
Thiazole | C3H6300NS – 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.80945-86-4, Name is 6-Bromo-2-chlorobenzothiazole, molecular formula is C7H3BrClNS. In a Patent，once mentioned of 80945-86-4, Computed Properties of C7H3BrClNS

Substituted imidazoles and thiazoles having the formula 1are useful for inhibiting farnesyltransferase. Also disclosed are farnesyltransferase-inhibiting compositions and methods of inhibiting farnesyltransferase in a patient.

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 80945-86-4 is helpful to your research., Computed Properties of C7H3BrClNS

Reference：
Thiazole | C3H10901NS – 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 4175-77-3, Name is 2,4-Dibromothiazole, Application In Synthesis of 2,4-Dibromothiazole.

A tetrazolinone compound represented by formula (1) [wherein Q represents a bivalent 5-membered aromatic heterocyclic group which may have at least one atom or group selected from the group P2; A represents a 5- to 10-membered monocyclic or condensed-cyclic heterocyclic group which may have at least one atom or group selected from the group P1; R1 and R2 independently represent a hydrogen atom or the like; R3 represents a C1-C6 alkyl group which may have at least one halogen atom or the like; R4, R5 and R6 independently represent a hydrogen atom or the like; and X represents an oxygen atom or a sulfur atom] has an excellent controlling effect on harmful organisms.

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 2,4-Dibromothiazole. In my other articles, you can also check out more blogs about 4175-77-3

Reference：
Thiazole | C3H1423NS – 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.2103-99-3, Name is 4-(4-Chlorophenyl)thiazol-2-amine, molecular formula is C9H7ClN2S. In a Patent，once mentioned of 2103-99-3, SDS of cas: 2103-99-3

The invention relates to a visible light to drive the synthetic 4 – alkyl or aryl – 2 – amino thiazole of the method, the method means that the olefin azide compound, ammonium thiocyanate and cupric acetate are added in the solvent acetonitrile, at a temperature of 25 C condition in order to wavelength is 450 nm – 460 nm visible light to drive the reaction, 20 – 36 H to obtain the reaction solution, the reaction solution the vane stem to obtain concentrate; the concentrate through silica gel column chromatography, to obtain the 4 – alkyl or aryl – 2 – aminothiazole. The invention high yield, mild condition, small pollution to the environment. (by machine translation)

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 2103-99-3 is helpful to your research., SDS of cas: 2103-99-3

Reference：
Thiazole | C3H10136NS – PubChem,
Thiazole | chemical compound | Britannica