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6332-57-6

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6332-57-6 Usage

Type of Compound

Heterocyclic compound

Structure

Imidazole ring fused to a pyridazine ring

Functional Groups

Two amine groups attached to carbon atoms 4 and 7

Potential Applications

Pharmaceutical industry

Biological Activity

Anticancer, antihypertensive, and anti-inflammatory properties

Research Significance

Unique structure and potential biological activities make it an interesting target for further research and development in the pharmaceutical field.

Check Digit Verification of cas no

The CAS Registry Mumber 6332-57-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6332-57:
(6*6)+(5*3)+(4*3)+(3*2)+(2*5)+(1*7)=86
86 % 10 = 6
So 6332-57-6 is a valid CAS Registry Number.

6332-57-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-imidazo[4,5-d]pyridazine-4,7-diamine

1.2 Other means of identification

Product number -
Other names 4,7-diamino-1H-imidazo<4,5-d>pyridazine

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:6332-57-6 SDS

6332-57-6Downstream Products

6332-57-6Relevant articles and documents

Hydrogen bond system generated by nitroamino rearrangement: New character for designing next generation energetic materials

Hu, Lu,Staples, Richard J.,Shreeve, Jean'Ne M.

, p. 603 - 606 (2021)

A new hydrogen bond system is formed by the transfer of a proton from nitroamino to form nitroimino. The proton and the oxygen in nitroimino form an intramolecular hydrogen bond and two intermolecular hydrogen bonds that shorten the distance between molecules both vertically and horizontally leading to higher density. This journal is

Acylation of heteroaromatic amines (I). Perbenzoylation of diaminopyridazines

Suzuki,Katou,Mitsuhashi

, p. 1451 - 1453 (2007/10/08)

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