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2-ACETYLAMINO-THIAZOLE-4-CARBOXYLIC ACID is a chemical compound with the molecular formula C7H7NO3S, belonging to the thiazole class of compounds. It features an acetylamine group and a carboxylic acid group, which contribute to its potential biological activities. 2-ACETYLAMINO-THIAZOLE-4-CARBOXYLIC ACID is widely recognized in pharmaceutical and medicinal research for its diverse applications, including antimicrobial, antibacterial, and antifungal properties.

50602-38-5

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50602-38-5 Usage

Uses

Used in Pharmaceutical and Medicinal Research:
2-ACETYLAMINO-THIAZOLE-4-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various drugs and pharmaceutical agents. Its unique chemical structure allows it to be a versatile building block for the development of new therapeutics.
Used in Antimicrobial Applications:
2-ACETYLAMINO-THIAZOLE-4-CARBOXYLIC ACID is used as an antimicrobial agent for its ability to inhibit the growth of various microorganisms, making it a valuable component in the fight against infections.
Used in Antibacterial Applications:
In the field of antibacterial research, 2-ACETYLAMINO-THIAZOLE-4-CARBOXYLIC ACID is utilized for its potential to combat bacterial infections, offering a possible alternative or adjunct to existing treatments.
Used in Antifungal Applications:
2-ACETYLAMINO-THIAZOLE-4-CARBOXYLIC ACID is used as an antifungal agent, targeting fungal pathogens and contributing to the development of treatments for fungal infections.
Used in the Synthesis of Therapeutic Agents:
2-ACETYLAMINO-THIAZOLE-4-CARBOXYLIC ACID is used as a precursor in the synthesis of various therapeutic agents, potentially leading to the discovery of new drugs for the treatment of a range of diseases and disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 50602-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,0 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50602-38:
(7*5)+(6*0)+(5*6)+(4*0)+(3*2)+(2*3)+(1*8)=85
85 % 10 = 5
So 50602-38-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O3S/c1-3(9)7-6-8-4(2-12-6)5(10)11/h2H,1H3,(H,10,11)(H,7,8,9)

50602-38-5SDS

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-acetamido-1,3-thiazole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-acetamido-4-thiazolecarboxylic acid

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:50602-38-5 SDS

50602-38-5Relevant academic research and scientific papers

Synthesis of lathyrane diterpenoid nitrogen-containing heterocyclic derivatives and evaluation of their anti-inflammatory activities

Wang, Wang,Xiong, Liangliang,Li, Yutong,Song, Zhuorui,Sun, Dejuan,Li, Hua,Chen, Lixia

, (2022/01/24)

As our ongoing work on lathyrane diterpenoid derivatization, three series of lathyrane diterpenoid derivatives were designed and synthesized based combination principles, including pyrazole, thiazole and furoxan moieties. Biological evaluation indicated t

N-(2 - (amine methyl) phenyl) thiazole-4-carboxamide derivatives and its preparation method and application (by machine translation)

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Paragraph 0014-0015; 0044-0045, (2016/11/17)

This invention involves a kind of N-(2 - (amine methyl) phenyl) thiazole-4-carboxamide derivatives and its preparation method and application. The N-(2 - (amine methyl) phenyl) thiazole-4-carboxamide derivatives having the general formula I is a compound

THIAZOLE DERIVATIVES AND THEIR USE AS VAP-1 INHIBITORS

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Page 47, (2010/02/07)

A compound of the formula (I): R1-NH-X-Y-Z (I) wherein R1 is acyl; X is a bivalent residue derived from optionally substituted thiazole; Y is a bond, lower alkylene or -COHN-; and Z is a groupe of the formulae (II) or (III) wherein R

Synthesis of methyl 2-acetylamino-5-(1,3-dithian-2-yl)thiazole-4-carboxylate

Feliu, Lidia,Ajana, Wadi,Joule, John A.,Lopez-Calahorra, Francisco,Alvarez, Mercedes

, p. 1299 - 1308 (2007/10/03)

The synthesis of methyl 2-acetylamino-5-(1,3-dithian-2-yl)thiazole-4-carboxylate (4) by formylation of a 4-substituted thiazole and then reaction with 1,3-propanedithiol are described. The utility of different ortho-directing groups (ODGs) for the lithiation of the thiazole 4-position has been studied.

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