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2-(4-PHENYL-1,3-THIAZOL-2-YL)ACETAMIDE is a chemical compound with the molecular formula C11H10N2OS. It is a thiazole derivative featuring a phenyl group attached to the thiazole ring. 2-(4-PHENYL-1,3-THIAZOL-2-YL)ACETAMIDE is an amide, characterized by the presence of both a thiazole ring and an acetamide group. Its structural features and potential biological activities suggest that it may have applications in pharmaceuticals and agrochemicals. Further research and studies are necessary to ascertain its specific uses and potential benefits across different fields.
Used in Pharmaceutical Industry:
2-(4-PHENYL-1,3-THIAZOL-2-YL)ACETAMIDE is used as a chemical intermediate for the development of pharmaceuticals due to its unique structural properties and potential to exhibit biological activities that could be beneficial in medicinal chemistry.
Used in Agrochemical Industry:
2-(4-PHENYL-1,3-THIAZOL-2-YL)ACETAMIDE is used as a building block in the synthesis of agrochemicals, where its structural features may contribute to the creation of effective compounds for agricultural applications, such as pesticides or herbicides.

58351-19-2

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58351-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58351-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,5 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58351-19:
(7*5)+(6*8)+(5*3)+(4*5)+(3*1)+(2*1)+(1*9)=132
132 % 10 = 2
So 58351-19-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2OS/c12-10(14)6-11-13-9(7-15-11)8-4-2-1-3-5-8/h1-5,7H,6H2,(H2,12,14)

58351-19-2SDS

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-(4-PHENYL-1,3-THIAZOL-2-YL)ACETAMIDE

1.2 Other means of identification

Product number -
Other names 4-Phenylthiazol-2-acetamid

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:58351-19-2 SDS

58351-19-2Relevant academic research and scientific papers

Alternative products in one-pot reaction of benzylidene-malononitrile, thiocarbamoylacetamide and halomethyl ketones

Krauze,Vijums,Sile,Duburs

experimental part, p. 239 - 244 (2010/07/10)

6-Oxo-5-(1,3-thiazol-2-yl)-1,4,5,6-tetrahydropyridine-3-carbonitriles 17, corresponding 6-oxo-5-(1,3-thiazol-2-yl)-5,6-dihydropyridine-3-carbonitriles 18 and intermediates - 2-(1,3-thiazol-2-yl)acetamides 15 and 4,4-dicyano-2-(1,3- thiazol-2-yl)-butyramides 16 have been obtained as alternative products to 3-hydroxy-2,3-dihydro-7H-thiazolo[3,2-a]pyridines 5 carrying out one-pot condensation of 2-thiocarbamoylacetamide 2, base 3, halomethyl ketones 4 and benzylidenemalononitrile 1.

Reactions with Monothiomalonamides: Synthesis of Polysubstituted Thiazoles

El-Reedy, A. M.,Hussain, S. M.,Youssef, M. M. M.

, p. 521 - 529 (2007/10/02)

Monothiomalonamides (1a, b) coupled with arenediazonium salts yield the α-arylhydrazone derivatives (2a-e).Reaction of 1a, b with α-haloketones afforded polysubstituted thiazoles 6a-e.Compounds 6 condensed with p-nitrosodimethylaniline and coupled with ar

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