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2,4-Imidazolidinedione, 5-(4-iodophenyl)-5-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58559-15-2

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58559-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58559-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,5 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58559-15:
(7*5)+(6*8)+(5*5)+(4*5)+(3*9)+(2*1)+(1*5)=162
162 % 10 = 2
So 58559-15-2 is a valid CAS Registry Number.

58559-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-iodophenyl)-5-phenylimidazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 2,4-Imidazolidinedione,5-(4-iodophenyl)-5-phenyl

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:58559-15-2 SDS

58559-15-2Relevant academic research and scientific papers

Microwave-assisted four-component reaction for the synthesis of a monothiohydantoin inhibitor of a fatty acid amide hydrolase

Gallienne, Estelle,Muccioli, Giulio G.,Lambert, Didier M.,Shipman, Michael

supporting information; experimental part, p. 6495 - 6497 (2009/04/06)

Monothiohydantoin 3a is made in seven steps from 1,4-diiodobenzene and is shown to be an inhibitor of fatty acid amide hydrolase (IC50 = 23.4 ± 1.1 μM). The key step in the sequence involves a microwave-assisted four-component reaction that makes the 5,5′-disubstituted hydantoin nucleus by the sequential formation of two C-C and two C-N bonds.

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