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4-Chloro-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine is a heterocyclic chemical compound characterized by a molecular formula of C8H4ClF3N2. It features a pyrrolopyridine structure with a chloro group at the 4-position and a trifluoromethyl group at the 5-position. This unique structure and its chemical properties render it a promising candidate for the synthesis of novel bioactive molecules and pharmaceutical compounds, making it valuable in drug discovery and development.

1196507-58-0

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1196507-58-0 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine is used as a key intermediate in the synthesis of new drugs for various therapeutic applications. Its unique structure allows for the development of bioactive molecules with potential therapeutic effects.
Used in Drug Discovery:
In the field of drug discovery, 4-Chloro-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine serves as a valuable chemical entity for the design and synthesis of innovative pharmaceutical compounds. Its heterocyclic nature and substituents contribute to the exploration of new chemical space for drug candidates.
Used in Medicinal Chemistry Research:
4-Chloro-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine is utilized as a building block in medicinal chemistry research to create new chemical entities with potential pharmacological properties. Its structural features facilitate the investigation of structure-activity relationships and the optimization of drug candidates.
Used in Chemical Synthesis:
As a versatile chemical compound, 4-Chloro-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine is employed in various chemical synthesis processes. Its reactivity and functional groups enable the formation of diverse chemical products for applications in different industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1196507-58-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,5,0 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1196507-58:
(9*1)+(8*1)+(7*9)+(6*6)+(5*5)+(4*0)+(3*7)+(2*5)+(1*8)=180
180 % 10 = 0
So 1196507-58-0 is a valid CAS Registry Number.

1196507-58-0 Well-known Company Product Price

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  • Aldrich

  • (ADE001104)  4-Chloro-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine  AldrichCPR

  • 1196507-58-0

  • ADE001104-1G

  • 9,342.45CNY

  • Detail

1196507-58-0SDS

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 4-Chloro-5-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names 4-chloro-5-trifluoromethyl-1H-pyrrolo[2,3-b]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:1196507-58-0 SDS

1196507-58-0Relevant academic research and scientific papers

1H-PYRROLO[2,3-B] PYRIDINE DERIVATIVES AND THEIR USE AS KINASE INHIBITORS

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Paragraph 0586, (2015/02/18)

The inventions relates to compounds of (I) and therapeutic uses thereof: (I) The terms Z, Y, and R1 are as defined in the claims.

1H-PYRROLO[2,3-B] PYRIDINE DERIVATIVES AND THEIR USE AS KINASE INHIBITORS

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Page/Page column 136; 137, (2013/08/15)

The inventions relates to compounds of (I) and therapeutic uses thereof : (I) The terms Z, Y, and R1 are as defined in the claims.

PYRROLOPYRIDINES AS KINASE INHIBITORS

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Page/Page column 99, (2009/12/23)

Compounds of Formula (I) are useful for inhibition of CHKl and/or CHK2. Methods of using compounds of Formula (I) and stereoisomers and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions are disclosed.

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