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81569-27-9

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81569-27-9 Usage

General Description

The chemical 4-Thiazolecarboxylicacid,2-chloro-5-(1-methylethyl)-,methylester(9CI) is an organic compound with the molecular formula C8H10ClNO2S. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. This chemical is known for its potential therapeutic properties and is being studied for its anti-inflammatory and antimicrobial effects. It is important to handle this chemical with caution as it may pose health risks if not properly handled or used.

Check Digit Verification of cas no

The CAS Registry Mumber 81569-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,6 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 81569-27:
(7*8)+(6*1)+(5*5)+(4*6)+(3*9)+(2*2)+(1*7)=149
149 % 10 = 9
So 81569-27-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10ClNO2S/c1-4(2)6-5(7(11)12-3)10-8(9)13-6/h4H,1-3H3

81569-27-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-chloro-5-propan-2-yl-1,3-thiazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 2-chloro-5-isopropyl-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:81569-27-9 SDS

81569-27-9Downstream Products

81569-27-9Relevant articles and documents

The Preparation of Thiazole-4- and -5-carboxylates, and an Infrared Study of their Rotational Isomers

Barton, Anne,Breukelman, Stephen P.,Kaye, Perry T.,Meakins, G. Denis,Morgan, David J.

, p. 159 - 164 (2007/10/02)

Convenient general procedures have been developed for preparing series of thiazole-4- and -5-carboxylates containing alkyl and halogeno substituents.While both series of esters show i.r. carbonyl doublets caused by rotational isomerism, the more intense absorptions of the 4-carboxylates are the lower wavenumber components, whereas those of the 5-carboxylates are the higher wavenumber components.In both series the stronger bands arise from the thermochemically more stable forms; identification of these forms as the carbonyl O,S-syn-s-trans rotamers is more certain with the 4-carboxylates than with the 5-carboxylates.

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