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3-Chloro-6-hydrazinyl-4-Methylpyridazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66530-56-1

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66530-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66530-56-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,3 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 66530-56:
(7*6)+(6*6)+(5*5)+(4*3)+(3*0)+(2*5)+(1*6)=131
131 % 10 = 1
So 66530-56-1 is a valid CAS Registry Number.

66530-56-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-chloro-5-methylpyridazin-3-yl)hydrazine

1.2 Other means of identification

Product number -
Other names 3-chloro-6-hydrazino-4-methylpyridazine

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:66530-56-1 SDS

66530-56-1Relevant academic research and scientific papers

ION CHANNEL MODULATORS

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Paragraph 00376, (2019/12/25)

The present invention is directed to, in part, fused heteroaryl compounds and compositions useful for preventing and/or treating a disease or condition relating to aberrant function of a voltage-gated, sodium ion channel, for example, abnormal late/persistent sodium current. Methods of treating a disease or condition relating to aberrant function of a sodium ion channel including neurological disorders (e.g., Dravet syndrome, epilepsy), pain, and neuromuscular disorders are also provided herein.

Nucleophilic substitution and lipophilicity - Structure relations in methylazolopyridazines

Katrusiak, Anna,Ratajczak-Sitarz, Malgorzata,Skierska, Urszula,Zinczenko, Wiktoria

, p. 1372 - 1386 (2007/10/03)

Syntheses of methyl[1,2,4]triazolo- or methyltetrazolopyridazine isomers, their separation and nucleophilic substitution with morpholine, dimethylamine and hydrazine have been described. The lipophilicity of the azolopyridazines has been measured and rela

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