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1167055-73-3

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1167055-73-3 Usage

General Description

4-Oxazolecarboxylic acid, 2-bromo- is a chemical compound with the molecular formula C5H3BrNO3. It is an oxazole derivative with a bromo substituent at the 2-position. 4-Oxazolecarboxylicacid, 2-broMo- is used in the synthesis of pharmaceuticals and agrochemicals. It is also used as a building block in organic synthesis. Additionally, it has potential applications in medicinal chemistry and drug discovery. This chemical compound has attracted attention for its interesting biological activities and potential use as a therapeutic agent.

Check Digit Verification of cas no

The CAS Registry Mumber 1167055-73-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,7,0,5 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1167055-73:
(9*1)+(8*1)+(7*6)+(6*7)+(5*0)+(4*5)+(3*5)+(2*7)+(1*3)=153
153 % 10 = 3
So 1167055-73-3 is a valid CAS Registry Number.

1167055-73-3SDS

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 2-Bromooxazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Bromo-1,3-oxazole-4-carboxylic acid

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:1167055-73-3 SDS

1167055-73-3Downstream Products

1167055-73-3Relevant articles and documents

Widely Exploited, Yet Unreported: Regiocontrolled Synthesis and the Suzuki–Miyaura Reactions of Bromooxazole Building Blocks

Solomin, Vitalii V.,Radchenko, Dmytro S.,Slobodyanyuk, Evgeniy Y.,Geraschenko, Oleksandr V.,Vashchenko, Bohdan V.,Grygorenko, Oleksandr O.

, p. 2884 - 2898 (2019/03/07)

An approach to synthesis of 2-, 4-, and 5-bromooxazoles is described. The method was optimized, and its scope was extended to all three isomeric parents, as well as various alkyl- and aryl-substituted bromooxazoles. It was found that direct regiocontrolled lithiation followed by reaction with electrophilic bromine source was common for all substrates and led exclusively to the target substituted 2-, 4- and 5-bromooxazoles on multigram scale. The utility of the multipurpose building blocks obtained in this work was demonstrated in the Suzuki–Miyaura cross-coupling reaction under parallel synthesis conditions.

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