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2-Amino-5-methyl-1,3-thiazol-4(5H)-one is a heterocyclic organic compound with the molecular formula C4H6N2OS. It features a thiazolone ring structure, which consists of a five-membered ring containing two sulfur atoms, one oxygen atom, and two carbon atoms. The compound has an amino group at the 2-position and a methyl group at the 5-position. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new drugs. Its unique structure and reactivity make it an interesting target for chemical research and development.

3805-14-9

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3805-14-9 Usage

Chemical compound

2-Amino-5-methyl-1,3-thiazol-4(5H)-one

Type

Heterocyclic organic compound

Structure

Contains a thiazole ring with an amino group and a methyl group attached

Applications

Pharmaceuticals, agrochemicals

Uses

Building block in synthesis of bioactive compounds, intermediate in production of corrosion inhibitors and dyes

Research focus

Potential therapeutic uses including as an anti-inflammatory and anti-cancer agent, potential use as a chiral auxiliary in asymmetric synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 3805-14-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,0 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3805-14:
(6*3)+(5*8)+(4*0)+(3*5)+(2*1)+(1*4)=79
79 % 10 = 9
So 3805-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N2OS/c1-2-3(7)6-4(5)8-2/h2H,1H3,(H2,5,6,7)

3805-14-9SDS

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-amino-5-methyl-1,3-thiazol-4-one

1.2 Other means of identification

Product number -
Other names 2-amino-5-methylthiazolin-4-one

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:3805-14-9 SDS

3805-14-9Relevant academic research and scientific papers

5-substituted 2,4-thiazolidinediones (thiohydantoins), pseudothiohydantoins, and propseudothiohydantoins for use as antiviral agents

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Page/Page column 9-10, (2020/06/03)

The present invention concerns the synthesis and use of formulations of 5-substituted 2, 4-thiazolidinediones, pseudothiohydantoins, and propseudothiohydantoins and 2, 4-thiazolidinediones metforminate salts for topical and systemic treatments of infections caused by herpes simplex viruses and varicella zoster viruses.

BENZAMIDE COMPOUNDS AS GLUCOKINASE ACTIVATORS AND THEIR PHARMACEUTICAL APPLICATION

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Page/Page column 50, (2011/09/14)

Benzamide compounds of formula (I), their stereoisomers, tautomers, prodrugs, pharmaceutically acceptable salts, polymorphs, solvates and formulations thereof useful as Glucokinase activators or modulators are disclosed. The disclosure further relates to

The Synthesis of Some Pyrimidinyl and Thiazolyl Ureas and Thioureas and Some Related Compounds

Hurst, Derek T.,Stacey, Anthony D.,Nethercleft, Mark,Rahim, Amjad,Harnden, Michael R.

, p. 1221 - 1229 (2007/10/02)

Some pyrimidin-2- and pyrimidin-4-amines were treated with isocyanates and isothiocyanates to give the corresponding disubstituted ureas or thioureas.A pyrimidin-2-amine is more reactive than a pyrimidin-4-amine in these reactions. 2-Aminothiazoles and th

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