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5-(3-Bromphenyl)hydantoin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79422-72-3

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79422-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79422-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,2 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79422-72:
(7*7)+(6*9)+(5*4)+(4*2)+(3*2)+(2*7)+(1*2)=153
153 % 10 = 3
So 79422-72-3 is a valid CAS Registry Number.

79422-72-3SDS

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-(3-Bromphenyl)hydantoin

1.2 Other means of identification

Product number -
Other names 5-(3-bromophenyl)-imidazolidin-2,4-dione

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:79422-72-3 SDS

79422-72-3Relevant academic research and scientific papers

Carboxylic acid amides having antithrombotic activity

-

, (2008/06/13)

Compounds with antithrombotic activity and factor Xa-inhibiting activity of the general formula: Exemplary are: (1) (L)-2-(5-carbamimidoyl-2-hydroxy-phenyl)-N-[3-methyl-4-(2-aminocarbonyl-pyrrolidin-1-yl-carbonyl)-phenyl]-acetamide, (2) 2-(5-carbamimidoyl

Synthesis of Antiproteolytically Active Nα-Arylsulphonylated Amidinophenylglycinamides

Wagner, G.,Voigt, B.,Lischke, Ingrid

, p. 467 - 470 (2007/10/02)

Several Nα-arylsulphonylated p- and m-amidinophenylglycinamides were prepared for the purpose of testing their efficacy as serine proteinase inhibitors.These compounds were obtained from the bromophenylhydantoins 1 and 2 via the bromophenylglycines 3 and

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