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5-Benzyl-5-phenylimidazolidine-2,4-dione is a chemical compound with the molecular formula C15H13N2O2. It is a white crystalline solid that belongs to the class of imidazolidine-2,4-dione derivatives. 5-BENZYL-5-PHENYLIMIDAZOLIDINE-2,4-DIONE is characterized by the presence of a benzyl group attached to the 5-position of the imidazolidine ring and a phenyl group at the same position. It is known for its potential applications in pharmaceuticals and as a building block in the synthesis of various organic compounds. The compound's structure provides a stable platform for further chemical modifications, making it a valuable intermediate in organic synthesis.

4927-43-9

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4927-43-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4927-43-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,2 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4927-43:
(6*4)+(5*9)+(4*2)+(3*7)+(2*4)+(1*3)=109
109 % 10 = 9
So 4927-43-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H14N2O2/c19-14-16(18-15(20)17-14,13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-10H,11H2,(H2,17,18,19,20)/t16-/m1/s1

4927-43-9SDS

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-BENZYL-5-PHENYLIMIDAZOLIDINE-2,4-DIONE

1.2 Other means of identification

Product number -
Other names 5-Benzyl-5-phenyl-imidazolidin-2,4-dion

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4927-43-9 SDS

4927-43-9Relevant academic research and scientific papers

Synthesis, structure, and solvatochromic properties of pharmacologically active 5-substituted 5-phenylhydantoins

Trisovic, Nemanja,Valentic, Natasa,Erovic, Marko,Dakovic-Sekulic, Tatjana,Uscumlic, Gordana,Juranic, Ivan

experimental part, p. 1227 - 1234 (2012/06/04)

A series of 5-substituted 5-phenylhydantoins was synthesized and their UV absorption spectra were recorded in the region 200-400 nm in selected solvents of different polarity. The effects of solvent dipolarity/polarizability and solvent-solute hydrogen-bonding interactions were analyzed by means of the linear solvation energy relationship concept proposed by Kamlet and Taft. The lipophilicities of the investigated hydantoins were estimated by calculation of their log P values. The quantitative relationship between the ratio of the contributions of specific solvent interactions and the corresponding lipophilicity parameter is discussed. The correlation equations were combined with the corresponding ED50 values and different physicochemical parameters to generate new equations that demonstrate the reasonable relationships between solute-solvent interactions and the structure-activity parameters. In order to determine a spectroscopic assignment of the absorption bands in different solvents, quantum chemical calculations were done. Springer-Verlag 2011.

Efficient synthesis of 5-arylmethyl-5-phenylimidazolidine-2,4-dione (or 5-arylmethyl-5-phenyl-2-thioxoimidazolidin-4-one) from chalcone oxides under ultrasound irradiation

Li, Ji-Tai,Xu, Xiao-Ya,Yin, Ying

experimental part, p. 198 - 201 (2012/04/04)

Synthesis of 5-arylmetlryl-5-phenylirnidazolidine-2,4-dione (or 5-arylmethyl-5-phenyl-2-thoxoimidazolidin-4- one) via the reaction of 3-aryl-2,3-epoxyl-1-phenyl-1-propanone and urea (or thiourea) was carried out in 57-98% yields at 50 °C in EtOH in the pr

Modified Bucherer-Bergs reaction for the one-pot synthesis of 5,5′-disubstituted hydantoins from nitriles and organometallic reagents

Montagne, Cyril,Shipman, Michael

, p. 2203 - 2206 (2007/10/03)

Diverse sets of 5,5′-disubstituted hydantoins can conveniently be made in moderate to good yields (40-92%) by a one-pot process involving treatment of aromatic, heteroaromatic or aliphatic nitriles with an organometallic reagent (RLi or RMgX) followed by

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