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131084-55-4 Usage

General Description

5-CHLORO-1H-PYRROLO[2,3-C]PYRIDINE is a chemical compound with the molecular formula C9H5ClN2. It is a heterocyclic compound containing a pyrrole ring fused to a pyridine ring with a chlorine atom at the 5-position. 5-CHLORO-1H-PYRROLO[2,3-C]PYRIDINE has potential applications in pharmaceuticals, agrochemicals, and materials science. It is commonly used as an intermediate in the synthesis of various organic compounds and can also act as a building block in the development of new drugs and agrochemicals. The 5-CHLORO-1H-PYRROLO[2,3-C]PYRIDINE has been the subject of research and development due to its unique structure and potential pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 131084-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,0,8 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 131084-55:
94 % 10 = 4
So 131084-55-4 is a valid CAS Registry Number.



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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017


1.1 GHS Product identifier

Product name 5-Chloro-1H-Pyrrolo[2,3-C]Pyridine

1.2 Other means of identification

Product number -
Other names 5-Chloro-1H-pyrrolo[2,3-c]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:131084-55-4 SDS

131084-55-4Relevant articles and documents

Heterocyclic compound as FGFR inhibitor, synthesis method and applications thereof


Paragraph 0165; 0168-0171, (2019/10/01)

The present invention discloses a heterocyclic compound as an FGFR inhibitor, and a synthesis method thereof, and applications of the heterocyclic compound in preparation of drugs for treating cancers. According to the present invention, the heterocyclic compound as the FGFR inhibitor or the pharmaceutically acceptable salt thereof has high FGFR inhibitory action, and the pharmaceutical composition prepared from the heterocyclic compound has good anticancer effect and wide application range.

New bicyclic compounds as crac channel modulators


, (2014/06/24)

The present invention relates to novel compounds which are inhibitors of CRAC channel activity. This invention also relates to pharmaceutical compositions containing them, process for their preparation and their use in therapy.



Page/Page column 42; 43, (2010/04/28)

The present invention relates to a compound of formula I: wherein: R1 is C1-6 alkyl, C3-8 cycloalkyl, aryl, heterocyclyl, or -COR1x, where the C1-6 alkyl, C3-8 cycloalkyl, aryl, and heterocyclyl may be substituted; and R1x is C3-8 cycloalkyl, aryl, or heterocyclyl, any of which may be substituted; R2, R3, R4, R5, R6, and R7 are each independently hydrogen, halogen, C1-6 alkyl, or aryl, where the C1-6 alkyl or aryl may be substituted; R8 is hydrogen, C1-6 alkyl, aryl, or heterocyclyl, any of which may be substituted; or a pharmaceutically acceptable salt or ester thereof.

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