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CAS

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6274-04-0

2,4-dimethyl-3-(2-oxo-2-phenylethyl)-1,3-thiazol-3-ium is a chemical compound characterized by the presence of a thiazole ring, a phenylethyl group, and two methyl groups. This positively charged ion is part of the thiazolium class of compounds, which are recognized for their wide range of biological activities such as antimicrobial, antiviral, and anticancer properties. The inclusion of the phenylethyl group in its structure indicates potential for pharmacological applications, as similar groups are prevalent in various drugs and bioactive molecules. 2,4-dimethyl-3-(2-oxo-2-phenylethyl)-1,3-thiazol-3-ium holds promise for use in medicinal chemistry and chemical biology due to its unique structural features and associated biological activities.

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  • 6274-04-0 Structure

  • Basic information

    1. Product Name: 2,4-dimethyl-3-(2-oxo-2-phenylethyl)-1,3-thiazol-3-ium
    2. Synonyms:
    3. CAS NO:6274-04-0
    4. Molecular Formula: Br*C13H14NOS
    5. Molecular Weight: 232.3208
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6274-04-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,4-dimethyl-3-(2-oxo-2-phenylethyl)-1,3-thiazol-3-ium(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-dimethyl-3-(2-oxo-2-phenylethyl)-1,3-thiazol-3-ium(6274-04-0)
    11. EPA Substance Registry System: 2,4-dimethyl-3-(2-oxo-2-phenylethyl)-1,3-thiazol-3-ium(6274-04-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 6274-04-0(Hazardous Substances Data)

6274-04-0 Usage

Uses

Used in Pharmaceutical Industry:
2,4-dimethyl-3-(2-oxo-2-phenylethyl)-1,3-thiazol-3-ium is used as a bioactive compound for its potential antimicrobial, antiviral, and anticancer properties. The presence of the phenylethyl group and the thiazolium ring may contribute to its effectiveness in targeting and treating various diseases and conditions.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,4-dimethyl-3-(2-oxo-2-phenylethyl)-1,3-thiazol-3-ium is utilized as a starting material or a scaffold for the development of new drugs. Its unique structure allows for modifications and the synthesis of derivative compounds that can be optimized for specific therapeutic applications.
Used in Chemical Biology:
2,4-dimethyl-3-(2-oxo-2-phenylethyl)-1,3-thiazol-3-ium serves as a tool in chemical biology for studying the interactions between small molecules and biological targets. Its ability to modulate biological activities can provide insights into the mechanisms of action and potential applications in biological research and drug discovery.

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

2-Methylthiazolium Salts as 1,4-Dinucleophiles. Thiazolopyridinium Salts from Westphal Condensation

Galera, C.,Vaquero, J. J.,Navio, Garcia J. L.,Alvarez-Builla, J.

, p. 1889 - 1892 (2007/10/02)

Condensation of 2-methylthiazolium salts with 1,2-dicarbonyls in the presence of base, yielded thiazolopyridinium derivatives.Results with different substrates are discussed.

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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