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144294-38-2

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144294-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 144294-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,2,9 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 144294-38:
(8*1)+(7*4)+(6*4)+(5*2)+(4*9)+(3*4)+(2*3)+(1*8)=132
132 % 10 = 2
So 144294-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3O2/c1-5-7(8(12)13)11-6(10-5)3-2-4-9-11/h2-4H,1H3,(H,12,13)

144294-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylimidazo[1,2-b]pyridazine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-methylimidazo<1,2-b>pyridazine-3-carboxylic acid

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:144294-38-2 SDS

144294-38-2Downstream Products

144294-38-2Relevant articles and documents

Research on heterocyclic compounds. XXX. Synthesis and pharmacological activity of 2-methylimidazo[1,2-b]pyridazine-3-carboxylic acids

Abignente,Arena,Luraschi,Saturnino,Rossi,Berrino,Cenicola

, p. 931 - 944 (2007/10/02)

A group of ethyl 2-methylimidazo[1,2-b]pyridazine-3-carboxylates were prepared by reaction in anhydrous ethanol of some substituted 3-aminopyridazines with ethyl 2-chloroacetoacetate. The corresponding carboxylic acids were obtained via alkaline or acid hydrolysis and then tested both in vivo to evaluate their antiinflammatory, analgesic and ulcerogenic actions and in vitro for their ability to inhibit the prostaglandin biosynthesis. The pharmacological results are discussed in terms of both structure-activity relationships and mechanism of action.

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