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6-CHLOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID is a chlorinated heterocyclic chemical compound with a molecular formula C8H5ClN2O2. It is a derivative of imidazo[1,2-a]pyridine and carboxylic acid, known for its potential applications in the synthesis of pharmaceuticals and agrochemicals. 6-CHLOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID plays a significant role in medicinal chemistry and drug discovery, particularly in the development of new treatments for various diseases. It also serves as a valuable research tool in the fields of chemical biology and bioorganic chemistry.

182181-19-7

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182181-19-7 Usage

Uses

Used in Pharmaceutical Industry:
6-CHLOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID is used as a key building block for the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the development of new drugs, potentially leading to the discovery of novel treatments for a wide range of diseases.
Used in Agrochemical Industry:
In the agrochemical industry, 6-CHLOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID is utilized as a starting material for the synthesis of various agrochemicals. Its properties make it suitable for the development of new pesticides, herbicides, and other agricultural chemicals, contributing to more effective and sustainable agricultural practices.
Used in Medicinal Chemistry Research:
6-CHLOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID is employed as a research tool in medicinal chemistry. Its unique structure and reactivity enable scientists to explore its potential in the development of new drug candidates, leading to advancements in the understanding of disease mechanisms and the discovery of innovative therapeutic approaches.
Used in Chemical Biology and Bioorganic Chemistry:
As a research tool in chemical biology and bioorganic chemistry, 6-CHLOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID is used to study the interactions between small molecules and biological systems. Its unique properties allow researchers to investigate its potential as a modulator of biological processes, providing insights into the development of new therapeutic agents and the understanding of complex biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 182181-19-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,1,8 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 182181-19:
(8*1)+(7*8)+(6*2)+(5*1)+(4*8)+(3*1)+(2*1)+(1*9)=127
127 % 10 = 7
So 182181-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H5ClN2O2/c9-5-1-2-7-10-6(8(12)13)4-11(7)3-5/h1-4H,(H,12,13)/p-1

182181-19-7 Well-known Company Product Price

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  • Alfa Aesar

  • (H50313)  6-Chloroimidazo[1,2-a]pyridine-2-carboxylic acid, 99%   

  • 182181-19-7

  • 250mg

  • 926.0CNY

  • Detail
  • Alfa Aesar

  • (H50313)  6-Chloroimidazo[1,2-a]pyridine-2-carboxylic acid, 99%   

  • 182181-19-7

  • 1g

  • 3334.0CNY

  • Detail

182181-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-CHLOROIMIDAZO[1,2-A]PYRIDINE-2-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 2-Carboxy-6-chloroimidazo[1,2-a]pyridine

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:182181-19-7 SDS

182181-19-7Downstream Products

182181-19-7Relevant academic research and scientific papers

AMINO-DIHYDROTHIAZINE AND AMINO-DIOXIDO DIHYDROTHIAZINE COMPOUNDS AS BETA-SECRETASE ANTAGONISTS AND METHODS OF USE

-

, (2014/05/07)

The present invention provides a new class of compounds useful for the modulation of beta-secretase enzyme (BACE) activity. The compounds have a general Formula I: wherein variables A4, A5, A6, A8, R1, R2, R3, R7 and n of Formula I, independently, are defined herein. The invention also provides pharmaceutical compositions comprising the compounds, and corresponding uses of the compounds and compositions for treatment of disorders and/or conditions related to A-beta plaque formation and deposition, resulting from the biological activity of BACE. Such BACE mediated disorders include, for example, Alzheimer's Disease, cognitive deficits, cognitive impairments, schizophrenia and other central nervous system conditions. The invention further provides compounds of Formula II and sub-formula embodiments thereof, intermediates and processes and methods useful for the preparation of compounds of Formulas I-II.

Fully automated continuous flow synthesis of highly functionalized imidazo[1,2-a] heterocycles

Herath, Ananda,Dahl, Russell,Cosford, Nicholas D.P.

supporting information; experimental part, p. 412 - 415 (2010/04/26)

[Chemical equation presented] The first continuous flow synthesis of imidazo[1,2-a]pyridine-2-carboxylic acids directly from 2-aminopyridines and bromopyruvic acid has been developed, representing a significant advance over the corresponding in-flask method. The process was applied to the multistep synthesis of imidazo[1,2-a]pyridine-2-carboxamides, including a Mur ligase inhibitor, using a two microreactor, multistep continuous flow process without isolation of intermediates.

IMIDAZO[1,2-A]PYRIDINES FOR THE TREATMENT OF CNS AND CARDIAC DISEASES

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, (2008/06/13)

The present invention relates to imidazo[1,2-a]pyridine compounds of formula (1) STR1 which are dopamine D-4 antagonists and useful as anti-psychotic agents.

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