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150162-48-4

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150162-48-4 Usage

General Description

2-(2,4-dichlorophenyl)thiazole-4-carbaldehyde, also known as DCTC, is an organic compound with the molecular formula C11H6Cl2N2OS. It is an aldehyde derivative with a thiazole ring and two chlorine atoms attached to the phenyl group. DCTC is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It is also used as a reagent in organic chemical reactions, particularly in the formation of thiazole derivatives. The compound is known for its strong odor and must be handled with care due to its potential irritant properties. DCTC has a wide range of applications in the field of organic chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 150162-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,1,6 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 150162-48:
(8*1)+(7*5)+(6*0)+(5*1)+(4*6)+(3*2)+(2*4)+(1*8)=94
94 % 10 = 4
So 150162-48-4 is a valid CAS Registry Number.

150162-48-4SDS

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-(2,4-dichlorophenyl)-1,3-thiazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-(2,4-DICHLOROPHENYL)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:150162-48-4 SDS

150162-48-4Upstream product

150162-48-4Relevant articles and documents

Synthesis of new 1,4-dihydropyridine derivatives containing thiazolyl substituents

Bazargan, Leila,Shafiee, Abbas,Amini, Mohsen,Dezfouli, Ebrahim Bakhshi,Azizi, Ebrahim,Ghaffari, Seyed Mahmood

scheme or table, p. 602 - 609 (2009/10/02)

A series of 4-[2-methyl (or aryl) thiazole-4-yl]-2,6-dimethyl-3,5-diacetyl (or dibenzoyl) 1,4-dihydropyridines were synthesized using a modified Hantzsch reaction involving the condensation of the corresponding aldehyde with acetyl acetone or benzoyl acetone. The preparation of the corresponding aldehydes (2-methylthiazole-4-carboxaldehyde and some 2-arylthiazole-4-carboxaldehydes) was achieved by a simplified protocol of the published synthesis.

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