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6-Benzylamino-7-deazapurine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60972-04-5

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60972-04-5 Usage

Chemical Properties

Tan Solid

Check Digit Verification of cas no

The CAS Registry Mumber 60972-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,7 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60972-04:
(7*6)+(6*0)+(5*9)+(4*7)+(3*2)+(2*0)+(1*4)=125
125 % 10 = 5
So 60972-04-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N4/c1-2-4-10(5-3-1)8-15-13-11-6-7-14-12(11)16-9-17-13/h1-7,9H,8H2,(H2,14,15,16,17)

60972-04-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Benzylamino-7-deazapurine

1.2 Other means of identification

Product number -
Other names N-benzyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine

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:60972-04-5 SDS

60972-04-5Downstream Products

60972-04-5Relevant academic research and scientific papers

4-chloro pyrrolo[2,3-d]pyrimidine substituted compound and synthetic method thereof

-

Paragraph 0040-0041; 0045, (2019/12/02)

The invention relates to a method for synthesizing 4-chloro pyrrolo[2,3-b] pyridine. The method mainly comprises three steps: 1) carrying out p-toluenesulfonyl chloride protection on a 4-chloro pyrrolo[2,3-d]pyrimidine compound; 2) reacting the 4-chloro p

Structure-based design, synthesis, and antimicrobial activity of purine derived SAH/MTA nucleosidase inhibitors

Tedder, Martina E.,Nie, Zhe,Margosiak, Stephen,Chu, Shaosong,Feher, Victoria A.,Almassy, Robert,Appelt, Krzysztof,Yager, Kraig M.

, p. 3165 - 3168 (2007/10/03)

The structure-based design, synthesis, and biological activity of novel inhibitors of S-adenosyl homocysteine/methylthioadenosine (SAH/MTA) nucleosidase are described. Using 6-substituted purine and deaza purines as the core scaffolds, a systematic and structure guided series of modifications provided low nM inhibitors with broad-spectrum antimicrobial activity.

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