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Imidazo[1,2-b]pyridazine-3-carboxylic acid, 6-chloro-2-methylis a chemical compound characterized by the molecular formula C9H6ClN3O2. It is a member of the pyridazine carboxylic acids, which are organic compounds featuring a pyridazine ring with a carboxylic acid group attached. The incorporation of a chloro and methyl group in its structure endows Imidazo[1,2-b]pyridazine-3-carboxylic acid, 6-chloro-2-methyl- with unique properties and reactivity, making it a versatile entity in pharmaceutical research and development, as well as in the synthesis of other organic compounds.

14714-22-8

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14714-22-8 Usage

Uses

Used in Pharmaceutical Research and Development:
Imidazo[1,2-b]pyridazine-3-carboxylic acid, 6-chloro-2-methylis utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Organic Synthesis:
Imidazo[1,2-b]pyridazine-3-carboxylic acid, 6-chloro-2-methylserves as a building block in the synthesis of other organic compounds, contributing to the advancement of organic chemistry and the creation of novel molecules with specific functions and properties.
Used in Chemical Research:
Imidazo[1,2-b]pyridazine-3-carboxylic acid, 6-chloro-2-methylis employed in chemical research to study its properties, reactivity, and potential applications in various chemical processes and reactions.
Used in Drug Design:
Imidazo[1,2-b]pyridazine-3-carboxylic acid, 6-chloro-2-methylis used as a template in drug design, where its structure can be modified to create new pharmaceutical agents with improved efficacy and selectivity for specific targets.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Imidazo[1,2-b]pyridazine-3-carboxylic acid, 6-chloro-2-methylis utilized to explore its potential as a lead compound for the development of new therapeutic agents, particularly in areas such as oncology, cardiovascular diseases, and neurological disorders.
Used in Chemical Industry:
Imidazo[1,2-b]pyridazine-3-carboxylic acid, 6-chloro-2-methylfinds applications in the chemical industry for the production of various chemical products, taking advantage of its unique chemical properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 14714-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,1 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14714-22:
(7*1)+(6*4)+(5*7)+(4*1)+(3*4)+(2*2)+(1*2)=88
88 % 10 = 8
So 14714-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClN3O2/c1-4-7(8(13)14)12-6(10-4)3-2-5(9)11-12/h2-3H,1H3,(H,13,14)

14714-22-8SDS

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 6-Chloro-2-methylimidazo[1,2-b]pyridazine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-chloro-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:14714-22-8 SDS

14714-22-8Downstream Products

14714-22-8Relevant academic research and scientific papers

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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