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1H-Purine-2,6-diamine, N,N'-bis(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39639-54-8

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39639-54-8 Usage

Derivative of purine

Heterocyclic aromatic organic compound

Diamine

Contains two amino groups

Bis(phenylmethyl)

Presence of two phenylmethyl groups

Synthesis

Used in the synthesis of various pharmaceuticals and organic compounds

Research interest

Fields of chemistry, pharmacology, and materials science

Check Digit Verification of cas no

The CAS Registry Mumber 39639-54-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,3 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39639-54:
(7*3)+(6*9)+(5*6)+(4*3)+(3*9)+(2*5)+(1*4)=158
158 % 10 = 8
So 39639-54-8 is a valid CAS Registry Number.

39639-54-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-N,6-N-dibenzyl-7H-purine-2,6-diamine

1.2 Other means of identification

Product number -
Other names N2,N6-dibenzyl-7(9)H-purine-2,6-diamine

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:39639-54-8 SDS

39639-54-8Downstream Products

39639-54-8Relevant academic research and scientific papers

Solution-phase synthesis of 2,6,9-trisubstituted purines

Fiorini, Maria T.,Abell, Chris

, p. 1827 - 1830 (2007/10/03)

A simple three-step method for the solution-phase combinatorial synthesis of 2,6,9-trisubstituted purines from 2,6-dichloropurine is described. The synthesis exploits the use of resin capture to remove excess reagent used in the final step.

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