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272773-11-2

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272773-11-2 Usage

General Description

3-Bromo-5-isoxazolecarboxylic acidmethylester is a chemical compound that is a derivative of isoxazolecarboxylic acid. It is a colorless liquid with a molecular formula of C6H5BrNO3 and a molecular weight of 214.012 g/mol. 3-Bromo-5-isoxazolecarboxylic acidmethylester is commonly used as a building block for the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also used as an intermediate in the synthesis of herbicides and plant growth regulators. 3-Bromo-5-isoxazolecarboxylic acidmethylester is known for its potential applications in the fields of medicine, agriculture, and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 272773-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,2,7,7 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 272773-11:
(8*2)+(7*7)+(6*2)+(5*7)+(4*7)+(3*3)+(2*1)+(1*1)=152
152 % 10 = 2
So 272773-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H4BrNO3/c1-9-5(8)3-2-4(6)7-10-3/h2H,1H3

272773-11-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-bromo-1,2-oxazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 3-bromo-5-isoxazolecarboxylate

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:272773-11-2 SDS

272773-11-2Relevant articles and documents

Design, synthesis and biological study of potent and covalent HER-2 tyrosine kinase inhibitors with low cytotoxicity in vitro

Jin, Shuyu,Sun, Xiuyun,Liu, Dan,Xie, Hua,Rao, Yu

, p. 1333 - 1345 (2019)

The discovery and development of a novel HER-2 tyrosine kinase inhibitor for the treatment of HER2-positive breast cancer are presented in this article. EGFR family has been recognized as a crucial meditator in the cancer progression; HER-2 tyrosine kinase was one of the members among them. In the effort to explore potent HER-2 inhibitors, a novel series of 4-anilino-3-cyanoquinoline derivatives have been designed, synthesized and evaluated. Most compounds possessed modest proliferation inhibition on SK-BR-3 cell line and HER-2 kinase. Compound 16 appeared to be the most potent compound (HER-2 kinase IC50: 19.4?nM, SK-BR-3 IC50: 94?nM). In the experiment of cellular cytotoxicity assay, compound 16 shows a much lower cytotoxicity than neratinib on Beas-2b cell line (Human bronchial epithelial cells). In conclusion, compound 16 would be a promising lead compound for further anti-breast cancer drug discovery.

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