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21869-84-1

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21869-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21869-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,6 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21869-84:
(7*2)+(6*1)+(5*8)+(4*6)+(3*9)+(2*8)+(1*4)=131
131 % 10 = 1
So 21869-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N5O/c1-2-3-13-4-10-6-5(13)7(14)12-8(9)11-6/h2,4H,1,3H2,(H3,9,11,12,14)

21869-84-1SDS

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 2-amino-7-prop-2-enyl-3H-purin-6-one

1.2 Other means of identification

Product number -
Other names 7-(2-Propenyl)guanin

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:21869-84-1 SDS

21869-84-1Downstream Products

21869-84-1Relevant articles and documents

Leonard,Frihart

, p. 5894,5899 (1974)

Use of purine compound in treatment or prevention of hyperuricemic or gouty diseases

-

Paragraph 0135; 0136; 0137, (2017/01/02)

The invention belongs to the technical field of medicines, relates to a use of a purine compound in treatment or prevention of hyperuricemic or gouty diseases, and concretely relates to a use of the purine compound concretely is a compound represented by formula (I), a pharmaceutically acceptable salt thereof, a solvate thereof or a composition containing anyone of the compound, the pharmaceutically acceptable salt and the solvate in the preparation of medicines for treating and/or preventing hyperuricemia, gouts, gouty inflammations and uratic nephropathy. In the formula (I), X represents a heteroaryl group selected from nitrogen-containing hetero atoms, Y represents a group selected from aryl groups or heteroaryl groups, the aryl groups or the heteroaryl groups are unsubstituted or are substituted with one or more halogen atoms or C-6 halogenated alkyl groups, m represents 3 or 4, and n represents 0 or 1.

Regioselective and efficient synthesis of N 7-substituted adenines, guanines, and 6-mercaptopurines

Maryska, Michal,Chudikova, Nadezda,Kotek, Vladislav,Dvorak, Dalimil,Tobrman, Tomas

, p. 501 - 507 (2013/07/26)

A simple and efficient protocol for the preparation of N 7-substituted adenines, guanines, and 6-mercaptopurines is described. The key step is the regioselective preparation of 7-substituted 6-chloropurines which are building blocks for the div

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