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21709-40-0

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21709-40-0 Usage

General Description

2-Amino-4-methyl-thiazole-5-carboxylic acid dimethylamide is a chemical compound with the molecular formula C6H10N4O2S. It is a derivative of thiazole, containing a carboxylic acid and dimethylamide functional group. 2-AMINO-4-METHYL-THIAZOLE-5-CARBOXYLIC ACID DIMETHYLAMIDE is commonly used as a building block in organic synthesis and pharmaceutical research. It is known for its diverse applications in the synthesis of pharmaceuticals, agrochemicals, and flavor compounds. 2-Amino-4-methyl-thiazole-5-carboxylic acid dimethylamide is a versatile chemical that plays a crucial role in the development of various useful products in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 21709-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,0 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21709-40:
(7*2)+(6*1)+(5*7)+(4*0)+(3*9)+(2*4)+(1*0)=90
90 % 10 = 0
So 21709-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H11N3OS/c1-4-5(6(11)10(2)3)12-7(8)9-4/h1-3H3,(H2,8,9)

21709-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-4-methyl-thiazole-5-carboxylic acid dimethylamide

1.2 Other means of identification

Product number -
Other names 2-amino-N,N,4-trimethyl-1,3-thiazole-5-carboxamide

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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More Details:21709-40-0 SDS

21709-40-0Downstream Products

21709-40-0Relevant articles and documents

Synthesis of 2,4,5-trisubstituted thiazoles with a 5-(N,N-dimethylaminomethyl) substituent

Stump, Bernhard,Kohler, Philipp C.,Schweizer, W. Bernd,Diederich, Francois

, p. 293 - 326 (2008/03/12)

We report synthetic strategies to 2,4,5-tri substituted thiazoles with a N,N- dimethylaminomethyl residue at C(5). Three different routes to build up these scaffolds are described. Furthermore, we report a retro-Brook rearrangement of a thiazole derivative as well as an unusual cyclization leading to a highly substituted benzothiazole.

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