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5-Methyl-4-thiazolecarboxylic acid methyl ester, also known as 4-Methyl-5-thiazolecarboxylic acid methyl ester, is an organic chemical compound with the molecular formula C6H7NO2S. It is a methyl ester derivative of 4-thiazolecarboxylic acid, characterized by its unique structure and properties. 5-Methyl-4-thiazolecarboxylic acid methyl ester is widely recognized for its versatility in the pharmaceutical industry, where it serves as a key intermediate in the synthesis of various drugs and pharmaceutical compounds. Its potential therapeutic applications in the treatment of different medical conditions make it a valuable asset in the development of new pharmaceuticals.

68751-05-3

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68751-05-3 Usage

Uses

Used in Pharmaceutical Industry:
5-Methyl-4-thiazolecarboxylic acid methyl ester is used as a key intermediate in the synthesis of various drugs and pharmaceutical compounds. Its unique structure and properties make it an essential building block in the development of new pharmaceuticals with potential therapeutic applications in the treatment of various medical conditions.
Used in Organic Synthesis:
As a versatile organic chemical compound, 5-Methyl-4-thiazolecarboxylic acid methyl ester is used as a building block in organic synthesis. Its reactivity and functional groups allow for the formation of a wide range of chemical products, contributing to the advancement of chemical research and development.
Used in Chemical Research:
5-Methyl-4-thiazolecarboxylic acid methyl ester is utilized in chemical research to explore its properties and potential applications. Its unique structure and reactivity make it an interesting subject for studying various chemical reactions and processes, further expanding the understanding of organic chemistry.
Used in Laboratory and Industrial Processes:
Due to its properties, 5-Methyl-4-thiazolecarboxylic acid methyl ester is suitable for use in various laboratory and industrial processes. Its versatility and reactivity make it a valuable component in the development of new processes and techniques, contributing to the progress of various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 68751-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,7,5 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68751-05:
(7*6)+(6*8)+(5*7)+(4*5)+(3*1)+(2*0)+(1*5)=153
153 % 10 = 3
So 68751-05-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO2S/c1-4-5(6(8)9-2)7-3-10-4/h3H,1-2H3

68751-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-methyl-1,3-thiazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 5-Methylthiazol-4-carbonsaeuremethylester

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:68751-05-3 SDS

68751-05-3Relevant articles and documents

CONTRASTING THERMAL BEHAVIOUR OF DIASTEREOISOMERIC 4-ACETYLTHIO-3-ACYLAMINO-1-(α-TRIPHENYLPHOSPHORANYLIDENE)ALKOXYCARBONYLMETHYLAZETIDIN-2-ONES

Irving, James R.,Perrone, Ettore,Stoodley, Richard J.

, p. 2501 - 2504 (2007/10/02)

Under conditions in which cis isomers of the title compounds are converted into 6β-acylamino-2-methylpenem-3-carboxylates, trans isomers afford thiazole-4-carboxylates and 2-alkyloxazolin-5-ones.

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