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5-chloro-4-fluoro-1H-pyrrolo[2,3-b]pyridine is a heterocyclic chemical compound with the molecular formula C7H4ClFN2. It features a pyrrolopyridine ring system and is utilized as a key building block in the synthesis of pharmaceuticals. 5-chloro-4-fluoro-1H-pyrrolo[2,3-b]pyridine is frequently employed in medicinal chemistry for the development of novel drugs and has been investigated for its potential antitumor, anti-inflammatory, and antimicrobial properties. Additionally, it serves as a reagent in organic synthesis, highlighting its diverse applications in chemical research and drug development.

1190317-94-2

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1190317-94-2 Usage

Uses

Used in Pharmaceutical Synthesis:
5-chloro-4-fluoro-1H-pyrrolo[2,3-b]pyridine is used as a building block for the creation of new drugs, leveraging its unique chemical structure to enhance the therapeutic potential of pharmaceutical compounds.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 5-chloro-4-fluoro-1H-pyrrolo[2,3-b]pyridine is utilized as a key component in the design and synthesis of drugs with potential antitumor, anti-inflammatory, and antimicrobial properties, contributing to the advancement of treatment options for various diseases.
Used in Organic Synthesis as a Reagent:
5-chloro-4-fluoro-1H-pyrrolo[2,3-b]pyridine serves as a versatile reagent in organic synthesis, enabling the development of a wide range of chemical compounds for use in various industries, including pharmaceuticals, materials science, and agrochemicals.
Used in Chemical Research and Drug Development:
5-chloro-4-fluoro-1H-pyrrolo[2,3-b]pyridine is integral to chemical research and drug development, where its unique properties and reactivity are harnessed to explore new chemical pathways and synthesize innovative therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 1190317-94-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,3,1 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1190317-94:
(9*1)+(8*1)+(7*9)+(6*0)+(5*3)+(4*1)+(3*7)+(2*9)+(1*4)=142
142 % 10 = 2
So 1190317-94-2 is a valid CAS Registry Number.

1190317-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Chloro-4-fluoro-1H-pyrrolo[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names 1H-PYRROLO[2,3-B]PYRIDINE,5-CHLORO-4-FLUORO

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:1190317-94-2 SDS

1190317-94-2Relevant academic research and scientific papers

AZAINDOLE CARBOXAMIDE COMPOUNDS FOR THE TREATMENT OF MYCOBACTERIAL INFECTIONS

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, (2021/04/02)

Provided herein are compounds of Formula (I) and Formula (II): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of tuberculosis.

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

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, (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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, (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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, (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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