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90004-07-2

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90004-07-2 Usage

General Description

Pyrido[2,3-d]pyridazin-5(6H)-one, 8-methyl- is a chemical compound with the molecular formula C9H8N2O. It is a bicyclic heterocyclic compound that consists of a pyridine ring fused to a diazinone ring. Pyrido[2,3-d]pyridazin-5(6H)-one, 8-methyl- is also known as 8-methylpyrido[2,3-d]pyridazin-5(6H)-one and is used in pharmaceutical research and drug development. It exhibits potential therapeutic properties and is being investigated for its potential use in the treatment of various diseases and conditions. Additionally, it has also been studied for its potential role as a building block in the synthesis of other biologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 90004-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,0 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90004-07:
(7*9)+(6*0)+(5*0)+(4*0)+(3*4)+(2*0)+(1*7)=82
82 % 10 = 2
So 90004-07-2 is a valid CAS Registry Number.

90004-07-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-methyl-6H-pyrido[2,3-d]pyridazin-5-one

1.2 Other means of identification

Product number -
Other names 8-Methyl-pyrido<2,3-d>pyridazinon-5

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:90004-07-2 SDS

90004-07-2Relevant articles and documents

Cyclotransformation in the series of fused 5-nitropyridin-2(1H)-ones

Smolyar,Yutilov

, p. 274 - 281 (2008)

Reactions with excess hydrazine hydrate of 5-nitropyridin-2(1H)-ones fused with benzene, pyridine, and 1,2,3-triazole rings led to a cyclotransformation of the 5-nitro-2-oxopyridine fragment into the 6-methyl-3-oxopyridazine structure. This cyclotransformation is of general character; a probable mechanism of the process is suggested. Details of the assumed mechanism were experimentally confirmed on model compounds.

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