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55644-07-0

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55644-07-0 Usage

Type of compound

Heterocyclic compound

Structure

Five-membered ring with oxygen and nitrogen atoms

Functional groups

Two cyano (CN) groups

Potential applications

Pharmaceutical and agricultural industries

Biological activity

Not specified in the material provided

Use

Building block for the synthesis of various pharmaceuticals and agrochemicals

Research and development

Candidate for further research in the field of organic chemistry

Industrial and scientific applications

Versatile compound with potential implications in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 55644-07-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,4 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55644-07:
(7*5)+(6*5)+(5*6)+(4*4)+(3*4)+(2*0)+(1*7)=130
130 % 10 = 0
So 55644-07-0 is a valid CAS Registry Number.

55644-07-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,5-oxadiazole-3,4-dicarbonitrile

1.2 Other means of identification

Product number -
Other names dicyanofurazan

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:55644-07-0 SDS

55644-07-0Downstream Products

55644-07-0Relevant articles and documents

Synthesis of 5-(1,2,5-oxadiazol-3-yl)-1H-etrazoles from 3-cyano-1,2,5-oxadiazoles

Godovikova,Vorontsova,Konyushkin,Firgang,Rakitin

, p. 406 - 409 (2009)

A number of 5-(1,2,5-oxadiazol-3-yl)-1H-tetrazoles were obtained in high yields by reactions of 3-cyano-1,2,5-oxadiazoles with sodium azide or by nitrosation of furazan-based amidrazones, which are easily prepared from the same starting reagents.

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