Tag: M.W:100-200

In an article, published in an article, once mentioned the application of 51640-36-9, Name is 2-Chlorothiazole-5-carbonitrile,molecular formula is C4HClN2S, is a conventional compound. this article was the specific content is as follows.HPLC of Formula: C4HClN2S

The present invention provides compounds of formula I and pharmaceutically acceptable salts thereof. The formula I compounds inhibit tyrosine kinase activity of JAK3, thereby making them useful for the treatment of inflammatory and autoimmune diseases.

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Reference：
Thiazole | C3H3172NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 6436-60-8, Name is Methyl 2-methylthiazole-4-carboxylate,molecular formula is C6H7NO2S, is a conventional compound. this article was the specific content is as follows.name: Methyl 2-methylthiazole-4-carboxylate

The asymmetric synthesis of a series of 3-thiazoline carboxylates, 2, was effected by MnO2 oxidation of the corresponding cis/trans thiazolidines, 1. The stereochemistry of the oxidation reaction was studied using NMR and chiral GC analyses. Compounds 2 were obtained with enantiomeric excesses (e.e.s) in the range of 40-100%.

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Reference：
Thiazole | C3H8449NS – PubChem,
Thiazole | chemical compound | Britannica

Application of 53266-94-7, 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. 53266-94-7, C7H10N2O2S. A document type is Patent, introducing its new discovery.

Disclosed are compounds of the general formula: wherein R1 is amino, an acylated amino or a protected amino group, X is hydrogen or methoxy, and R” is hydrogen, R or R4 wherein R is an organic residue attached to the azetidine ring through a carbon atom therein and R4 is azido, a halogen, an amino group which may optionally be acylated or a group of the formula ¿OR5, or ¿S-S-R5 wherein R5 is an organic residue and n is 0, 1 or 2, and pharmaceutically acceptable salts and esters thereof. The compounds have antimicrobial and/or beta-lactamase-inhibitory activity and are of value as drugs for human beings and domesticated animals

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Reference：
Thiazole | C3H10778NS – PubChem,
Thiazole | chemical compound | Britannica

Electric Literature of 1235406-42-4. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 1235406-42-4, Name is tert-Butyl thiazol-4-ylcarbamate

The invention provides a compound of formula: or a salt thereof, wherein the variables RAA, n, ring A, ring B, R1a, R1b, R2, R3, R4, R5, R6, R7, R8, and R9 have the meaning as described herein, and compositions containing such compounds and methods for using such compounds and compositions.

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Reference：
Thiazole | C3H9111NS – 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. 2602-85-9, Name is Benzo[d]thiazole-2-carbonitrile, molecular formula is C8H4N2S. In a Article，once mentioned of 2602-85-9, name: Benzo[d]thiazole-2-carbonitrile

The synthetic route to and a preliminary biological evaluation of novel indolo[1,2-c]quinazolines (8) and benzimidazo[1,2-c]quinazolines (9) are described. The products were obtained by condensation of the appropriate diamines (e.g. 2-(2-aminophenyl)indole or 2-(2-aminophenyl)benzimidazole) with 2-cyanobenzothiazoles. This work further demonstrates the general applicability of microwaves for a facile and rapid access to original heterocycles with potential pharmaceutical value.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.name: Benzo[d]thiazole-2-carbonitrile. In my other articles, you can also check out more blogs about 2602-85-9

Reference：
Thiazole | C3H7519NS – 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.79265-30-8, Name is 2-(Trimethylsilyl)thiazole, molecular formula is C6H11NSSi. In a Article，once mentioned of 79265-30-8, Recommanded Product: 79265-30-8

The adduct derived from 2,3-O-isopropylidene-D-glyceraldehyde and 2-(trimethylsilyl)thiazole is readily converted into the title D-erythrose (50% overal yield) by selective protection of the hydroxy groups and cleavage of the thiazole ring; the D-threose derivative is obtained from the former by base-catalyzed epimerization at C-2. Wittig olefination of the D-erythrose derivative followed by Michael addition of benzylamine and aldehyde liberation from the thiazole ring leads to the amino sugar 2-deoxykanosamine (methyl 6-O-benzyl-3-benzylamino-2,3-dideoxy-alpha-D-arabinopyranoside) in 50% overall yield.

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 79265-30-8 is helpful to your research., Recommanded Product: 79265-30-8

Reference：
Thiazole | C3H1079NS – 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.28620-12-4, Name is 6-Nitro-2-benzothiazolinone, molecular formula is C7H4N2O3S. In a Patent，once mentioned of 28620-12-4, Quality Control of: 6-Nitro-2-benzothiazolinone

The present invention concerns derivatives of heteroarylsulfonamides, notably as blockers of Kv potassium channels, and more particularly of channels Kv1.5, Kv4.3 or Kv11.1, their application in clinical therapy and their preparation methods. These compounds correspond to the following general formula (I): where R1 represents one or more substituents of the phenyl core X such as: hydrogen, halogen, trifluoromethyl, trifluoromethoxy, linear or branched C1 -C4 alkyl, or linear or branched C1 -C4 alkoxy, represents oxygen or sulphur, B represents nitrogen when n= 1 or 2 and D represents -C(=O)-, or B represents CH when n=0 and D represents -CH2O- or when n=1 and D represents -O-, R2 represents a hydrogen, a methyl, a fluorine or chlorine atom or a methoxy, HetAr represents a pyridyl or quinolyl group, possibly substituted by a group such as a linear or branched C1-C4 alkyl, a linear or branched C1 -C4 alkoxy, a halogen, or a trifluoromethyl, and to their pharmaceutically acceptable salts

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 28620-12-4 is helpful to your research., Quality Control of: 6-Nitro-2-benzothiazolinone

Reference：
Thiazole | C3H7290NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route of 19989-66-3. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 19989-66-3, Name is Benzo[d]thiazol-6-ylmethanol

The present invention relates to novel spiro-oxadiazoline compounds that are suitable as agonists or partial agonists of a7-nAChR, and pharmaceutical compositions of the same, methods of preparing these compounds and compositions, and the use of these compounds and compositions in methods of maintaining, treating and/or improving cognitive function. In particular, methods of administering a spiro-oxadiazoline cx7-nAChR agonist or partial agonist, to a patient in need thereof, for example a patient with a cognitive deficiency and/or a desire to enhance cognitive function, that may derive a benefit therefrom.

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Reference：
Thiazole | C3H7506NS – 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.1826-11-5, Name is 2-Phenylthiazole, molecular formula is C9H7NS. In a Article，once mentioned of 1826-11-5, Application In Synthesis of 2-Phenylthiazole

Several new iridium complexes with substituted 2-phenylthiazoles as the cyclometalated ligands have been synthesized and characterized to try to investigate the effect of the size of the pi system and substituent groups on physical properties. The complexes have the general structure of (C?N)2Ir(acac), where the C?N are 2-phenylthiazole (ptz), 2-(4-methylphenyl)thiazole (mptz), 2-(4-ethylphenyl)thiazole (eptz). The absorption, emission, cyclic voltammetry and thermostability of the complexes were systematically investigated. The experimental results revealed that the maximum emission wavelength in CH2Cl2 at room temperature are in the range 542-547 nm, which is blue shift than that of the known iridium(III) bis(2-phenylbenzothiazolato-N,C2?) acetyl acetonate (bt)2Ir(acac) due to decreasing the size of the pi system in the benzothiazole portion of 2-phenylbenzothiazole ligand.

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 1826-11-5 is helpful to your research., Application In Synthesis of 2-Phenylthiazole

Reference：
Thiazole | C3H3933NS – PubChem,
Thiazole | chemical compound | Britannica

1603-91-4, Name is 4-Methylthiazol-2-amine, molecular formula is C4H6N2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 1603-91-4, SDS of cas: 1603-91-4

1H-pyrrolo[2,3-c]pyridine-7-carboxamides constitute a new series of allosteric mGluR5 antagonists. Variation of the substituents attached to the heterocyclic scaffold allowed to improve the physico-chemical parameters for optimization of the aqueous solubility while retaining high in vitro potency.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.SDS of cas: 1603-91-4. In my other articles, you can also check out more blogs about 1603-91-4

Reference：
Thiazole | C3H9956NS – PubChem,
Thiazole | chemical compound | Britannica