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Imidazo[1,2-b]pyridazine-2-carboxamide (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123531-29-3

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123531-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123531-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,5,3 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 123531-29:
(8*1)+(7*2)+(6*3)+(5*5)+(4*3)+(3*1)+(2*2)+(1*9)=93
93 % 10 = 3
So 123531-29-3 is a valid CAS Registry Number.

123531-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name imidazo[1,2-b]pyridazine-2-carboxamide

1.2 Other means of identification

Product number -
Other names Imidazo[1,2-b]pyridazine-2-carboxamide (9CI)

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:123531-29-3 SDS

123531-29-3Downstream Products

123531-29-3Relevant academic research and scientific papers

Research on heterocyclic compounds. XXXVIII. Synthesis and pharmacological activity of imidazo[1,2-b]pyridazine-2-carboxylic derivatives

Luraschi,Arena,Sacchi,Laneri,Abignente,Avallone,D'Amico,Berrino,Rossi

, p. 213 - 217 (2007/10/03)

A series of imidazo[1,2-b]pyridazine-2-carboxylic acids, esters and amides was synthesized and tested for antiinflammatory, analgesic and ulcerogenic activities. The ethyl esters were prepared by cyclocondensation of some 3-aminopyridazines with ethyl bromopyruvate, followed by hydrolysis or ammonolysis in order to obtain the corresponding acids and amides. The inhibitory activity on the carrageenaninduced edema in the rat paw and on writhes induced by acetic acid in mice was evaluated, as well as the ulcerogenic action on the rat gastric mucosa. The pharmacological activity was discussed in terms of structure-activity relationships. In particular, the analgestic activity shown by these carboxylic derivatives was compared with that found in other series of imidazo[1,2-b]pyridazine analogues previously examined.

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