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2-[(4-bromophenyl)amino]-3,7-dihydro-6H-purin-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123994-72-9

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123994-72-9 Usage

Type of compound

Purine derivative

Usage

Pharmaceutical intermediate in drug synthesis

Potential pharmacological activities

Antitumor, antiviral properties

Molecular structure

Bromophenyl group attached to a purine ring

Importance

Valuable in medicinal chemistry

Possible applications

Development of new therapeutic agents

Check Digit Verification of cas no

The CAS Registry Mumber 123994-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,9,9 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 123994-72:
(8*1)+(7*2)+(6*3)+(5*9)+(4*9)+(3*4)+(2*7)+(1*2)=149
149 % 10 = 9
So 123994-72-9 is a valid CAS Registry Number.

123994-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-bromoanilino)-3,7-dihydropurin-6-one

1.2 Other means of identification

Product number -
Other names N2-(p-bromophenyl)guanine

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:123994-72-9 SDS

123994-72-9Downstream Products

123994-72-9Relevant academic research and scientific papers

Interaction of GTP Derivatives with Cellular and Oncogenic ras-p21 Proteins

Noonan, Timothy,Brown, Neal,Dudycz, Lech,Wright, George

, p. 1302 - 1307 (2007/10/02)

A series of N2-substituted quanosine 5'-triphosphates was synthesized from the corresponding nucleosides.The nucleosides were prepared by treatment of N2-substituted guanines with tetra-O-acetylribose under conditions which maximized

Structure-Activity Relationships of N2-Substituted Guanines as Inhibitors of HSV1 and HSV2 Thymidine Kinases

Hildebrand, Catherine,Sandoli, Daniele,Focher, Federico,Gambino, Joseph,Ciarrocchi, Giovanni,et al.

, p. 203 - 206 (2007/10/02)

A series of N2-phenylguanines was synthesized and tested for inhibition of the thymidine kinases encoded by Herpes simplex viruses type 1 and type 2.Compounds with hydrophobic, electron-attracting groups in the meta position of the phenyl ring

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