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113366-46-4

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113366-46-4 Usage

Synthesis Reference(s)

Tetrahedron Letters, 28, p. 3585, 1987 DOI: 10.1016/S0040-4039(00)95542-4

Check Digit Verification of cas no

The CAS Registry Mumber 113366-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,6 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 113366-46:
(8*1)+(7*1)+(6*3)+(5*3)+(4*6)+(3*6)+(2*4)+(1*6)=104
104 % 10 = 4
So 113366-46-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO2S/c1-3-5-8-4(2)6(11-5)7(9)10/h3H2,1-2H3,(H,9,10)

113366-46-4 Well-known Company Product Price

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  • Aldrich

  • (CBR00267)  2-Ethyl-4-methyl-1,3-thiazole-5-carboxylic acid  AldrichCPR

  • 113366-46-4

  • CBR00267-1G

  • 2,575.17CNY

  • Detail

113366-46-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-4-methyl-1,3-thiazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-Thiazolecarboxylicacid,2-ethyl-4-methyl

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:113366-46-4 SDS

113366-46-4Relevant articles and documents

Regioselectivity in the Lithiation of Methyl-substituted Thiazole- and Oxazole-Carboxylic Acids and Carboxamides: General Methods for the Elaboration of Trisubstituted Thiazoles and Oxazoles

Cornwall, Philip,Dell, Colin P.,Knight, David W.

, p. 2417 - 2428 (2007/10/02)

A number of anionic intermediates have been developed which are suitable for the elaboration of trisubstituted thiazoles and oxazoles.Thus, deprotonation of 2,4-dimethylthiazole-5-carboxylic acid 9 using either BuLi or LDA occurs regiospecifically at the

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