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64068-07-1

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64068-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64068-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,6 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64068-07:
(7*6)+(6*4)+(5*0)+(4*6)+(3*8)+(2*0)+(1*7)=121
121 % 10 = 1
So 64068-07-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClN3O2/c9-6-1-2-7-10-5(3-8(13)14)4-12(7)11-6/h1-2,4H,3H2,(H,13,14)

64068-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(6-chloroimidazo[1,2-b]pyridazin-2-yl)acetic acid

1.2 Other means of identification

Product number -
Other names -

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:64068-07-1 SDS

64068-07-1Downstream Products

64068-07-1Relevant academic research and scientific papers

Research on heterocyclic compounds. XXXIII-synthesis and analgesic activity of imidazo[1,2-b]pyridazine-2-acetic acid derivatives

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

, p. 349 - 354 (2007/10/02)

A series of imidazo[1,2-b]pyridazine-2-acetic esters, acids 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 4-chloroacetoacetate, followed by hydrolysis or amminolysis in order to obtain the corresponding acids and amides. The capacity of inhibiting the sarrageenan-induced edema in the rat paw and the writhes induced by acetic acid in mice were evaluated, as well as the ulcerogenic action in rats. The acid is derivatives showed significant analgesic activity which is comparable to that found in other series of imidazo[1,2-b]pyridazine analogs previously examined.

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