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31785-05-4

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31785-05-4 Usage

General Description

5-Amino-2-methyl-thiazole-4-carboxylic acid ethyl ester is a chemical compound with the molecular formula C8H10N2O2S. It is an ethyl ester derivative of 5-amino-2-methylthiazole-4-carboxylic acid. 5-AMINO-2-METHYL-THIAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used in organic synthesis as a reagent for the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. Its presence in various products and applications highlights its importance as a versatile intermediate in the synthesis of a wide range of compounds. Additionally, it is known for its potential biological activities, making it a significant molecule in medicinal chemistry research. Overall, 5-amino-2-methyl-thiazole-4-carboxylic acid ethyl ester is a valuable chemical in the field of organic synthesis and pharmaceutical development.

Check Digit Verification of cas no

The CAS Registry Mumber 31785-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,8 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31785-05:
(7*3)+(6*1)+(5*7)+(4*8)+(3*5)+(2*0)+(1*5)=114
114 % 10 = 4
So 31785-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O2S/c1-3-11-7(10)5-6(8)12-4(2)9-5/h3,8H2,1-2H3

31785-05-4 Well-known Company Product Price

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  • Aldrich

  • (SYX00062)  5-Amino-2-methylthiazole-4-carboxylic acid ethyl ester  AldrichCPR

  • 31785-05-4

  • SYX00062-1G

  • 3,540.42CNY

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31785-05-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Amino-2-methylthiazole-4-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names ethyl 5-amino-2-methyl-1,3-thiazole-4-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:31785-05-4 SDS

31785-05-4Downstream Products

31785-05-4Relevant articles and documents

Discovery of a Pyrimidothiazolodiazepinone as a Potent and Selective Focal Adhesion Kinase (FAK) Inhibitor

Groendyke, Brian J.,Nabet, Behnam,Mohardt, Mikaela L.,Zhang, Haisheng,Peng, Ke,Koide, Eriko,Coffey, Calvin R.,Che, Jianwei,Scott, David A.,Bass, Adam J.,Gray, Nathanael S.

, p. 30 - 38 (2021/01/11)

Focal adhesion kinase (FAK) is a tyrosine kinase with prominent roles in protein scaffolding, migration, angiogenesis, and anchorage-independent cell survival and is an attractive target for the development of cancer therapeutics. However, current FAK inhibitors display dual kinase inhibition and/or significant activity on several kinases. Although multitargeted activity is at times therapeutically advantageous, such behavior can also lead to toxicity and confound chemical-biology studies. We report a novel series of small molecules based on a tricyclic pyrimidothiazolodiazepinone core that displays both high potency and selectivity for FAK. Structure-activity relationship (SAR) studies explored modifications to the thiazole, diazepinone, and aniline "tail,"which identified lead compound BJG-03-025. BJG-03-025 displays potent biochemical FAK inhibition (IC50 = 20 nM), excellent kinome selectivity, activity in 3D-culture breast and gastric cancer models, and favorable pharmacokinetic properties in mice. BJG-03-025 is a valuable chemical probe for evaluation of FAK-dependent biology.

Rearrangement of 4-(Aminothiocarbonyl)oxazoles to 5-Aminothiazoles. Synthetic and MINDO/3 MO Studies

Corrao, Stephanie L.,Macielag, Mark J.,Turchi, Ignatius J.

, p. 4484 - 4487 (2007/10/02)

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