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1032815-07-8

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1032815-07-8 Usage

Structure

Pyrrolopyridine derivative with a chloro-substituted phenylsulfonyl group attached to the 4-position on the pyrrolopyridine ring

Potential applications

Medicinal chemistry (pharmaceuticals and agrochemicals development), drug discovery and development research

Unique structure

Valuable building block for the synthesis of various organic compounds

Functional groups

Chloro, phenylsulfonyl, pyrrolopyridine, carboxaldehyde

Interaction with biological targets

Of interest for research in drug discovery and development

Check Digit Verification of cas no

The CAS Registry Mumber 1032815-07-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,8,1 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1032815-07:
(9*1)+(8*0)+(7*3)+(6*2)+(5*8)+(4*1)+(3*5)+(2*0)+(1*7)=108
108 % 10 = 8
So 1032815-07-8 is a valid CAS Registry Number.

1032815-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-5-carbaldeh yde

1.2 Other means of identification

Product number -
Other names 4-chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde

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:1032815-07-8 SDS

1032815-07-8Relevant articles and documents

DERIVATIVES OF AN FGFR INHIBITOR

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, (2021/06/11)

The present disclosure relates to derivatives (e.g., hydroxyl, keto, glucuronide, sulfonic acid, and deuterated) of a Fibroblast Growth Factor Receptors (FGFR) inhibitor, including methods of preparation thereof, and intermediates in the preparation thereof, which are useful in the treatment of FGFR mediated disease such as cancer.

SUBSTITUTED TRICYCLIC COMPOUNDS AS FGFR INHIBITORS

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Page/Page column 216; 217, (2014/01/18)

The present invention relates to tricyclic compounds, and pharmaceutical compositions of the same, that are inhibitors of one or more FGFR enzymes and are useful in the treatment of FGFR-associated diseases such as cancer.

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