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92422-79-2

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92422-79-2 Usage

General Description

2-M-TOLYL-THIAZOLE-4-CARBALDEHYDE is an organic compound with a molecular formula C12H11NOS. It is a yellow to orange solid with a melting point of 88-92°C. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a building block in the manufacturing of dyes, pigments, and various functional materials. Additionally, 2-M-TOLYL-THIAZOLE-4-CARBALDEHYDE has been studied for its potential biological and pharmacological activities, including its antimicrobial and antifungal properties. Overall, this chemical has diverse industrial applications and continues to be of interest for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 92422-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,2 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92422-79:
(7*9)+(6*2)+(5*4)+(4*2)+(3*2)+(2*7)+(1*9)=132
132 % 10 = 2
So 92422-79-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NOS/c1-8-3-2-4-9(5-8)11-12-10(6-13)7-14-11/h2-7H,1H3

92422-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methylphenyl)-1,3-thiazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-M-tolyl-thiazole-4-carbaldehyde

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:92422-79-2 SDS

92422-79-2Relevant articles and documents

Heterocycles 38. Biocatalytic synthesis of new heterocyclic mannich bases and derivatives

Leonte, Denisa,Bencze, László Csaba,Paizs, Csaba,Irimie, Florin Dan,Zaharia, Valentin

, p. 12300 - 12313 (2015/08/18)

This paper describes the biocatalytic synthesis of new Mannich bases containing various heterocyclic rings (thiazole, furane, thiophene, pyridine) by applying the lipase catalyzed trimolecular condensation of the corresponding heterocyclic aldehydes with acetone and primary aromatic amines, in mild and eco-friendly reaction conditions. The obtained Mannich bases were acylated to their corresponding N-acetyl derivatives. All compounds were characterized by 1H-NMR, 13C-NMR and MS spectrometry.

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