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2-(2-BROMO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is a chemical compound with the molecular formula C12H9BrNO3. It is an ester derivative of oxazole-4-carboxylic acid, containing a bromo-phenyl group. Its unique structural properties and functional groups make it a valuable tool for the development of new molecules with potential biological activity.
Used in Pharmaceutical Industry:
2-(2-BROMO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used as a building block and intermediate for the synthesis of various organic compounds, including pharmaceutical drugs. It is also used in research and development for the production of new chemical entities.
Used in Organic Synthesis:
2-(2-BROMO-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is used as a precursor for further chemical transformations. Its ethyl ester functionality makes it suitable for use in organic synthesis reactions.

885274-67-9

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885274-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 885274-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 885274-67:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*4)+(2*6)+(1*7)=219
219 % 10 = 9
So 885274-67-9 is a valid CAS Registry Number.

885274-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2-bromophenyl)-1,3-oxazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names -

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

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

More Details:885274-67-9 SDS

885274-67-9Downstream Products

885274-67-9Relevant academic research and scientific papers

Synthesis and Biological Investigation of Oxazole Hydroxamates as Highly Selective Histone Deacetylase 6 (HDAC6) Inhibitors

Senger, Johanna,Melesina, Jelena,Marek, Martin,Romier, Christophe,Oehme, Ina,Witt, Olaf,Sippl, Wolfgang,Jung, Manfred

, p. 1545 - 1555 (2016)

Histone deacetylase 6 (HDAC6) catalyzes the removal of an acetyl group from lysine residues of several non-histone proteins. Here we report the preparation of thiazole-, oxazole-, and oxadiazole-containing biarylhydroxamic acids by a short synthetic proce

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