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4-Imidazolidinone, 5-methylene-3-phenyl-2-thioxo-, also known as 3-Phenyl-5-methylene-2-thioxo-4-imidazolidinone, is a chemical compound with the molecular formula C10H8N2OS. It is a heterocyclic compound, specifically an imidazolidinone derivative, featuring a five-membered imidazolidinone ring with a methylene group at the 5-position, a phenyl group at the 3-position, and a thioxo group at the 2-position. 4-Imidazolidinone, 5-methylene-3-phenyl-2-thioxo- is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a building block for more complex molecules. Its structure and properties make it a versatile intermediate for the synthesis of various biologically active compounds.

5789-27-5

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5789-27-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5789-27-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,8 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5789-27:
(6*5)+(5*7)+(4*8)+(3*9)+(2*2)+(1*7)=135
135 % 10 = 5
So 5789-27-5 is a valid CAS Registry Number.

5789-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methylidene-3-phenyl-2-sulfanylideneimidazolidin-4-one

1.2 Other means of identification

Product number -
Other names 4-Imidazolidinone,5-methylene-3-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:5789-27-5 SDS

5789-27-5Downstream Products

5789-27-5Relevant academic research and scientific papers

A convenient synthesis of 3-aryl-5-methylidene-2-thiohydantoins

Kukushkin, Maxim E.,Karpov, Nikita A.,Shybanov, Dmitry E.,Zyk, Nikolai V.,Beloglazkina, Elena K.

, p. 126 - 128 (2022/03/08)

3-Aryl-5-methylidene-2-thiohydantoins were constructed in one-pot reaction of aryl isothiocyanates and 3-morpholino- alanine in alkaline medium with the subsequent treatment with boiling hydrochloric acid.

Preparation and chemical properties of 5-dialkylaminomethylhydantoins and 2-thio-analogues

Fujisaki, Fumiko,Shoji, Kaori,Sumoto, Kunihiro

experimental part, p. 1415 - 1420 (2010/04/29)

An efficient procedure for the preparation of 5- dialkylaminomethylhydantoins 3, which are easily obtained from cyclization of the corresponding urea derivatives 2 starting with β-aminoalanines 1, is described. Methylenehydantoin and the corresponding 2-t

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