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4-Imidazolidinone, 3-(3-methylphenyl)-2-thioxo-, also known as 3-(3-Methylphenyl)-2-thioxo-4-imidazolidinone, is a chemical compound with the molecular formula C10H10N2OS. It is a derivative of imidazolidinone, featuring a 3-methylphenyl group attached to the imidazolidinone ring and a thioxo group at the 2-position. 4-Imidazolidinone, 3-(3-methylphenyl)-2-thioxo- is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a chemical intermediate. Its structure and properties make it a subject of study for researchers exploring the synthesis and reactivity of heterocyclic compounds.

61388-77-0

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61388-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61388-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,8 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61388-77:
(7*6)+(6*1)+(5*3)+(4*8)+(3*8)+(2*7)+(1*7)=140
140 % 10 = 0
So 61388-77-0 is a valid CAS Registry Number.

61388-77-0SDS

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 3-(3-methylphenyl)-2-sulfanylideneimidazolidin-4-one

1.2 Other means of identification

Product number -
Other names 2-Thioxo-3-m-tolyl-imidazolidin-4-on

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:61388-77-0 SDS

61388-77-0Relevant academic research and scientific papers

Microwave-assisted synthesis of 3,5-disubstituted thiohydantoins using functional ionic liquid as soluble support

Zhuo, Chen,Xian, Dong,Hui, Xie,Mei, Li

experimental part, p. 1121 - 1127 (2011/06/17)

A new approach for the syntheses of 3,5-disubstituted thiohydantoins was described using functionalized ionic liquid as soluble support. The products were obtained in good yields and purities after cyclization-cleavage from the ionic-liquid-supported under microwave irradiation, the ionic-liquid-supported species can there be purified from the reaction mixture by simple washing, and no chromatographic purification were needed during the synthesis. The Japan Institute of Heterocyclic Chemistry.

Traceless approach for the synthesis of 3,5-disubstituted thiohydantoins on functionalized ionic-liquid support

Yao, Chao,Zhang, Yandong,Zhang, Guolin,Chen, Wenteng,Yu, Yongping,Houghten, Richard A.

scheme or table, p. 717 - 724 (2011/03/19)

A traceless approach for the synthesis of 3,5-disubstituted thiohydantoins on a novel functionalized ionic-liquid support, 5, is described. Acylation of benzylamine functionalized ionic-liquid support with amino acids yielded ionic-liquid-supported amino acids, which reacted with isothiocyanates to afford ionic-liquid-supported thioureas. Following intramolecular cyclization cleavage from the ionic-liquid support by trifluoroacetic acid (TFA), the desired 3,5-disubstituted thiohydantoins were obtained in good yields and purities. The efficiency of this ionic-liquid-phase strategy facilitated isolation and analysis of intermediates and removal of excess reagents and by-products during the reaction process.

A New Method of Synthesis of 3-Monosubstituted-2-thiohydantoins and -Hydantoins

Ryczek, J.

, p. 2599 - 2604 (2007/10/02)

A new method of synthesis of 3-monosubstituted derivatives of 2-thiohydantoin and hydantoin in reaction of isothiocyanate or isocyanate glycin ethyl ester with primary aliphatic and aromatic amines has been described. Crude products were obtained with high yield and purity. The structure of these compounds was confirmed by spectral methods. Key words: 2-thiohydantoin, hydantoin, isothiocyanate glycin ethyl ester, isocyanate glycin ethyl ester

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