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449758-25-2

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449758-25-2 Usage

Physical form

White to off-white powder

Common uses

Intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Chemical properties

Acts as a ligand in metal-organic coordination chemistry

Potential applications

Anti-cancer agent, treatment of tuberculosis, materials science and nanotechnology

Unique properties

Diverse applications and subject of research in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 449758-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,9,7,5 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 449758-25:
(8*4)+(7*4)+(6*9)+(5*7)+(4*5)+(3*8)+(2*2)+(1*5)=202
202 % 10 = 2
So 449758-25-2 is a valid CAS Registry Number.

449758-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(tetrazol-1-yl)benzonitrile

1.2 Other means of identification

Product number -
Other names 2-Tetrazol-1-yl-benzonitrile

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:449758-25-2 SDS

449758-25-2Relevant articles and documents

1,6 - SUBSTITUTED (3R,6R) -3- (2,3-DIHYDRO-1H-INDEN-2-YL)-2,5-PIPERAZINEDIONE DERIVATIVES AS OXYTOCIN RECEPTOR ANTAGONISTS FOR THE TREATMENT OF PRE-TERM LABOUR, DYSMENORRHEA AND ENDOMETRIOSIS

-

Page/Page column 59, (2008/06/13)

The present invention relates to compound S of Formula (I).

Thrombin inhibitors

-

, (2008/06/13)

Compounds of the invention are useful in inhibiting thrombin and associated thrombotic occlusions having the following structure: wherein R1 is, for example, hydrogen, Cl, or cyano, and R2 is, for example, hydrogen,

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