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139022-25-6

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139022-25-6 Usage

General Description

Imidazo[1,2-a]pyridine-6-carboxylic acid (IPCA) is a chemical compound that belongs to the class of organic compounds known as imidazopyridines which are aromatic compounds containing an imidazo ring fused to a pyridine ring. It is characterized by a fused ring system that includes a pyridine ring and an imidazole ring. IPCA has applications in areas of medicinal chemistry due to its bioactive properties. IMIDAZO[1,2-A]PYRIDINE-6-CARBOXYLIC ACID is used as a scaffold structure in the synthesis of various pharmaceuticals, highlighting its importance in medicinal chemistry and drug design. It exhibits anti-inflammatory, antiviral, and anticancer activities, and combines properties of both imidazole and pyridine moieities, thereby making it a crucial component in pharmaceutical development.

Check Digit Verification of cas no

The CAS Registry Mumber 139022-25-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,0,2 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 139022-25:
(8*1)+(7*3)+(6*9)+(5*0)+(4*2)+(3*2)+(2*2)+(1*5)=106
106 % 10 = 6
So 139022-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O2/c11-8(12)6-1-2-7-9-3-4-10(7)5-6/h1-5H,(H,11,12)

139022-25-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H33128)  Imidazo[1,2-a]pyridine-6-carboxylic acid, 95%   

  • 139022-25-6

  • 1g

  • 1056.0CNY

  • Detail
  • Alfa Aesar

  • (H33128)  Imidazo[1,2-a]pyridine-6-carboxylic acid, 95%   

  • 139022-25-6

  • 5g

  • 4222.0CNY

  • Detail

139022-25-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Imidazo[1,2-a]pyridine-6-carboxylic Acid

1.2 Other means of identification

Product number -
Other names Imidazo[1,2-a]pyridine-6-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:139022-25-6 SDS

139022-25-6Relevant articles and documents

PROCESS FOR PREPARATION OF SAVOLITINIB AND ITS INTERMEDIATES

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Page/Page column 30, (2021/11/20)

The present application relates to a process for preparation of chiral amine fragment (IV) of savolitinib. The present application also relates to a process for preparation of savolitinib using the chiral amine (IV), as prepared by the process of the present application. The present application also discloses new intermediates useful for the synthesis of savolitinib. The present application further relates to crystalline forms of savolitinib, namely AA1, formic acid solvate and AA2. The present application also relates to amorphous solid dispersion of savolitinib.

P2X3 AND/OR P2X2/3 COMPOUNDS AND METHODS

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Paragraph 0287-0289, (2018/04/17)

The present disclosure provides novel compounds and methods for preparing and using these compounds. In one embodiment, the compounds are of the structure of formula (I), wherein R1-R7 are defined herein. In a further embodiment, these compounds are useful in method for regulating one or both of the P2X3 or P2X2/3 receptors. In another embodiment, these compounds are useful for treating pain in patients by administering one or more of the compounds to a patient. In another embodiment, these compounds are useful for treating respiratory dysfunction in patients by administering one or more of the compounds to a patient.

AMIDO SPIROCYCLIC AMIDE AND SULFONAMIDE DERIVATIVES

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Page/Page column 143, (2013/09/12)

Provided are amido spirocyclic amide and sulfonamide compounds, pharmaceutical compositions comprising such compounds, and methods of treatment using such compounds.

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