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172678-68-1

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172678-68-1 Usage

General Description

5-Thiazolecarboxylic acid, 2-phenyl-, methyl ester is a chemical compound that belongs to the class of thiazolecarboxylic acids. It is commonly used as an intermediate for the synthesis of various pharmaceuticals and organic compounds. The methyl ester form of this compound makes it more stable and easier to handle in laboratory settings. It is also known for its wide range of applications in the field of medicinal chemistry and drug development. Additionally, it possesses potential biological activities that make it a valuable compound for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 172678-68-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,6,7 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 172678-68:
(8*1)+(7*7)+(6*2)+(5*6)+(4*7)+(3*8)+(2*6)+(1*8)=171
171 % 10 = 1
So 172678-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2S/c1-14-11(13)9-7-12-10(15-9)8-5-3-2-4-6-8/h2-7H,1H3

172678-68-1SDS

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 methyl 2-phenyl-1,3-thiazole-5-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Phenyl-thiazole-5-carboxylic acid methyl ester

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:172678-68-1 SDS

172678-68-1Upstream product

172678-68-1Downstream Products

172678-68-1Relevant articles and documents

Synthesis of substituted oxazoles from enamides

Panda, Niranjan,Mothkuri, Raghavender

, p. 5727 - 5735 (2015/01/16)

Annulation of enamides into 2,5- and 2,4,5-substituted oxazoles by NBS/Me2S in the presence of mild base has been achieved. The reaction conditions are simple and tolerant to a wide variety of substituents including both electron-donating and withdrawing groups to produce oxazoles in one-pot without further purification of the intermediate.

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