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6824-10-8

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6824-10-8 Usage

General Description

"(2E)-2-(5H-purin-6-ylmethylidene)hydrazinecarbothioamide" is a chemical compound with the molecular formula C9H8N6S. It is a hydrazinecarbothioamide derivative with a purine group attached to a methylidene moiety. (2E)-2-(5H-purin-6-ylmethylidene)hydrazinecarbothioamide has potential biological activities that make it a subject of interest in pharmaceutical research. Its structure suggests that it could potentially interact with proteins or enzymes in living organisms. Additionally, this compound may have properties that could make it useful in the development of new drugs or therapies. Further research is needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 6824-10-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,2 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6824-10:
(6*6)+(5*8)+(4*2)+(3*4)+(2*1)+(1*0)=98
98 % 10 = 8
So 6824-10-8 is a valid CAS Registry Number.

6824-10-8SDS

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 Purine-6-carboxaldehyde, thiosemicarbazone

1.2 Other means of identification

Product number -
Other names 9H-PURINE-6-CARBALDEHYDE

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:6824-10-8 SDS

6824-10-8Upstream product

6824-10-8Downstream Products

6824-10-8Relevant articles and documents

Preparation and properties of a 6- and 2.6-substituted purine

Giner-Sorolla

, p. 611 - 618 (2007/10/05)

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