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5-phenyl-2-thioxo-4-imidazolidinone is a heterocyclic organic compound with the molecular formula C9H8N2OS. It features a thioxo group and an imidazolidinone ring, making it a versatile chemical with a wide range of applications in pharmaceuticals and organic synthesis.

62420-76-2

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62420-76-2 Usage

Uses

Used in Pharmaceutical Synthesis:
5-phenyl-2-thioxo-4-imidazolidinone is used as a starting material for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Agricultural Chemicals:
In the agricultural industry, 5-phenyl-2-thioxo-4-imidazolidinone is utilized as a starting material for the synthesis of different agricultural chemicals, contributing to the development of effective pest control and crop protection solutions.
Used as a Reagent in Organic Synthesis:
5-phenyl-2-thioxo-4-imidazolidinone is employed as a reagent in organic synthesis to introduce the imidazolidinone moiety into other molecules. This enhances the properties of the target compounds and expands the scope of organic chemistry.
Used in Biological Research:
5-phenyl-2-thioxo-4-imidazolidinone has been investigated for its potential biological activities, including antifungal, antibacterial, and antiproliferative properties. This research opens up possibilities for new treatments and applications in the fields of medicine and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 62420-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,2 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62420-76:
(7*6)+(6*2)+(5*4)+(4*2)+(3*0)+(2*7)+(1*6)=102
102 % 10 = 2
So 62420-76-2 is a valid CAS Registry Number.

62420-76-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenyl-2-thioxoimidazolidin-4-one

1.2 Other means of identification

Product number -
Other names 4-IMIDAZOLIDINONE,5-PHENYL-2-THIOXO-

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:62420-76-2 SDS

62420-76-2Relevant academic research and scientific papers

Chemoselective synthesis of biheterocyclic skeletons tetrahydro-1H-pyrrolo[1,2-c]imidazole and tetrahydropyrrolo[1,2-c]thiazole derivatives via multicomponent self-sorting domino strategy

Cai, Qun,Jia, Feng-Cheng,Li, Deng-Kui,Xu, Cheng,Ding, Ke-Rong,Wu, An-Xin

, p. 6104 - 6111 (2015)

Abstract A highly efficient chemoselective synthesis of multifunctionalized tetrahydro-1H-pyrrolo[1,2-c]imidazole and tetrahydropyrrolo[1,2-c]thiazole derivatives has been established from arylglyoxal monohydrates, nitriles, and thioureas. A series of control experiments suggested that this reaction proceeded through the convergent integration of two self-sorting domino sequences. This synthetic strategy is promising for diversity-oriented synthesis of alkaloid analogues.

Synthesis of new 2,5-diamino-1,3-thiazole and 2-thiohydantoin derivatives by condensation of N-(2-Aryl-1-chloro-2-oxoethyl) carboxamides with thioureas

Balya,Chernega,But,Vasilenko,Brovarets,Drach

experimental part, p. 1427 - 1435 (2009/02/07)

N-(2-Aryl-1-chloro-2-oxoethyl) carboxamides react under mild conditions with thiourea, N-alkyl-and N-arylthioureas, and various N,N′-disubstituted thioureas, following the Hantzsch reaction scheme. The reactions are selective, and the resulting 2,5-diamin

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