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89715-82-2

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89715-82-2 Usage

General Description

5-HYDRAZINO-6-AZAURACIL is a chemical compound with the molecular formula C4H5N5O. It is a purine analog and a potential antineoplastic agent. 5-HYDRAZINO-6-AZAURACIL may have the ability to block the conversion of inosine monophosphate (IMP) to xanthosine monophosphate (XMP), inhibiting the synthesis of guanosine nucleotides and ultimately disrupting DNA and RNA production in cancer cells. 5-HYDRAZINO-6-AZAURACIL is currently being researched for its potential use in cancer treatment and as an antiviral agent.

Check Digit Verification of cas no

The CAS Registry Mumber 89715-82-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,1 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89715-82:
(7*8)+(6*9)+(5*7)+(4*1)+(3*5)+(2*8)+(1*2)=182
182 % 10 = 2
So 89715-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H5N5O2/c4-6-1-2(9)5-3(10)8-7-1/h4H2,(H,6,7)(H2,5,8,9,10)

89715-82-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hydrazinyl-2H-1,2,4-triazine-3,5-dione

1.2 Other means of identification

Product number -
Other names 1,2,4-Triazine-3,5(2H,4H)-dione,6-hydrazinyl

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:89715-82-2 SDS

89715-82-2Upstream product

89715-82-2Downstream Products

89715-82-2Relevant articles and documents

Derivatives of 3,5-dihydroxy-1,2,4-triazines (6-azauracil) with apparent cytostatic action.

CRISTESCU,MARCUS

, p. 135 - 137 (2007/10/05)

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