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130120-68-2

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130120-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130120-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,1,2 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 130120-68:
(8*1)+(7*3)+(6*0)+(5*1)+(4*2)+(3*0)+(2*6)+(1*8)=62
62 % 10 = 2
So 130120-68-2 is a valid CAS Registry Number.

130120-68-2SDS

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-amino-6,8-dichloropurine

1.2 Other means of identification

Product number -
Other names 6,8-dichloro-9H-Purin-2-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:130120-68-2 SDS

130120-68-2Downstream Products

130120-68-2Relevant articles and documents

Chemical process for the preparation of purine derivatives

-

, (2008/06/13)

A process for the preparation of a compound of formula (I) STR1 which process comprises reacting a compound of formula (II): STR2 wherein the amino group is optionally protected, with a side chain intermediate of formula (III): STR3 wherein Q is a leaving group, Rx and Ry are protected hydroxymethyl or acyloxymethyl, or group(s) convertible to hydroxymethyl or acyloxymethyl; and Rz is hydrogen or a group convertible thereto; and thereafter converting the 6- and 8- chloro substituents to hydrogen by means of reduction; converting Rx and Ry when other than hydroxymethyl or acyloxymethyl, to hydroxymethyl or acyloxymethyl, optionally converting Rx /Ry hydroxymethyl to acyloxymethyl or vice versa, deprotecting the 2-amino group where necessary and converting Rz, (when other than hydrogen) to hydrogen; and optionally forming a pharmaceutically acceptable salt thereof.

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