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3-Bromo-5-isoxazolecarboxylic acidmethylester is a colorless liquid chemical compound, a derivative of isoxazolecarboxylic acid, with a molecular formula of C6H5BrNO3 and a molecular weight of 214.012 g/mol. It is recognized for its potential applications across various fields, including medicine, agriculture, and chemical research, primarily serving as a building block for the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.

272773-11-2

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272773-11-2 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-5-isoxazolecarboxylic acidmethylester is used as a key building block for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of a wide range of medicinal compounds with diverse therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Bromo-5-isoxazolecarboxylic acidmethylester is utilized as an intermediate in the synthesis of herbicides and plant growth regulators. Its incorporation into these products helps enhance their effectiveness in controlling weeds and promoting plant growth, thereby improving agricultural productivity.
Used in Chemical Research:
3-Bromo-5-isoxazolecarboxylic acidmethylester is employed as a valuable intermediate in chemical research, enabling the exploration of new chemical reactions and the synthesis of novel organic compounds. Its versatility and reactivity make it a useful tool for advancing scientific understanding and developing innovative applications in the chemical domain.

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 academic research and scientific papers

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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