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38956-79-5

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38956-79-5 Usage

Uses

3-Hydrazinyl-6-methylpyridazine is used in preparation of 2-(3-oxo-2H,3H-[1,2,4]triazolo[4,3-b]pyridazin-2-yl)acetamide and 2-(3-oxo-[1,2,4]triazolo[4,3-a]pyrimidin-2-yl)acetamide derivatives as GPR139 receptor modulators.

Check Digit Verification of cas no

The CAS Registry Mumber 38956-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,9,5 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 38956-79:
(7*3)+(6*8)+(5*9)+(4*5)+(3*6)+(2*7)+(1*9)=175
175 % 10 = 5
So 38956-79-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N4/c1-4-2-3-5(7-6)9-8-4/h2-3H,6H2,1H3,(H,7,9)

38956-79-5SDS

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 3-Hydrazinyl-6-methylpyridazine

1.2 Other means of identification

Product number -
Other names 3-Methylpyridazin-6-Ylhydrazine

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:38956-79-5 SDS

38956-79-5Relevant articles and documents

BICYCLIC TRIAZOLES AS PROTEIN KINASE MODULATORS

-

Page/Page column 107, (2008/12/05)

The present disclosure provides bicyclic triazole protein kinase modulators and methods of using these compounds to treat diseases mediated by kinase activity.

Hydrazination of Pyridazines and Phthalazines

Counotte-Potman, A.,Plas, H. C. van der

, p. 1259 - 1261 (2007/10/02)

It is shown by 15N-labelling techniques that hydrazination of pyridazines partly occurs according to a reaction pathway, involving addition of the nucleophile (hydrazine), ring opening and ring closure (SN(ANRORC)-mechanism).It is also proved that phthalazines undergo hydrazination without ring opening (SN(AE)-mechanism).

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