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6274-04-0

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6274-04-0 Usage

General Description

2,4-dimethyl-3-(2-oxo-2-phenylethyl)-1,3-thiazol-3-ium is a chemical compound with a thiazole ring and a phenylethyl group, along with two methyl groups. It is a positively charged ion due to the thiazolium group. Thiazolium compounds are known for their diverse biological activities, including antimicrobial, antiviral, and anticancer properties. The presence of the phenylethyl group suggests potential pharmacological activities, as this type of group is commonly found in drugs and other bioactive compounds. 2,4-dimethyl-3-(2-oxo-2-phenylethyl)-1,3-thiazol-3-ium may have potential applications in medicinal chemistry and chemical biology.

Check Digit Verification of cas no

The CAS Registry Mumber 6274-04-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6274-04:
(6*6)+(5*2)+(4*7)+(3*4)+(2*0)+(1*4)=90
90 % 10 = 0
So 6274-04-0 is a valid CAS Registry Number.

6274-04-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,4-dimethyl-1,3-thiazol-3-ium-3-yl)-1-phenylethanone,bromide

1.2 Other means of identification

Product number -
Other names HMS2844P03

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:6274-04-0 SDS

6274-04-0Relevant articles and documents

Method and composition for rejuvinating cells, tissues organs, hair and nails

-

, (2008/06/13)

In one embodiment, the present invention relates to compounds and compositions including pharmaceutical compositions containing the compounds and associated methods that uncouple sugar-mediated coupling of proteins, lipids, nucleic acids, and other biomat

Routes to Pyrrolothiazoles. Rotational Isomerism of Pyrrolo-thiazole-5-carbaldehydes

Brindley, Jocelyn C.,Gillon, David G.,Meakins, Denis G.

, p. 1255 - 1260 (2007/10/02)

Four 3,6-disubstituted pyrrolothiazoles (one containing a 3-aryl group) were prepared from 2,4-disubstituted thiazoles by the known method, and this work clarified some confusion in the literature.A new route, involving substitution into the thiazo

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