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6312-66-9

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6312-66-9 Usage

General Description

2,2'-(7H-purin-6-ylazanediyl)diethanol is a chemical compound with the molecular formula C12H16N6O2. It is a purine derivative, which means it contains a double-ring structure of nitrogen and carbon atoms. 2,2'-(7H-purin-6-ylazanediyl)diethanol is also classified as a diethanolamine, indicating that it contains two hydroxyethyl groups. The presence of the purine and diethanolamine groups makes this chemical suitable for use as a building block in pharmaceuticals and organic synthesis. It may also have potential applications in the development of nucleoside analogs and other bioactive molecules. Further research and evaluation of its properties are necessary to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 6312-66-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6312-66:
(6*6)+(5*3)+(4*1)+(3*2)+(2*6)+(1*6)=79
79 % 10 = 9
So 6312-66-9 is a valid CAS Registry Number.

6312-66-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-hydroxyethyl(7H-purin-6-yl)amino]ethanol

1.2 Other means of identification

Product number -
Other names Bis-(2-hydroxy-aethyl)-(7(9)H-purin-6-yl)-amin

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:6312-66-9 SDS

6312-66-9Downstream Products

6312-66-9Relevant articles and documents

Synthesis and biological evaluation of nitrogen mustard derivatives of purine bases

Bo?ns, Benjamin,Azouz, Mounir,Ouk, Tan-Sothea,Zerrouki, Rachida

, p. 69 - 80 (2013)

This paper deals with the synthesis of nitrogen mustard analogs, derivatives of purine bases. Alkylation in position N-9 and diethanolamine fixation on position 6 were managed by microwave irradiations. Chlorination of these dihydroxylated intermediates led to a cyclization, giving tricyclic purine base analogs bearing a chloroethyl chain. Finally, MTT assays on obtained compounds do not show cytotoxicity on four different cancer cell lines.

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