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1204501-41-6

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1204501-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1204501-41-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,5,0 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1204501-41:
(9*1)+(8*2)+(7*0)+(6*4)+(5*5)+(4*0)+(3*1)+(2*4)+(1*1)=86
86 % 10 = 6
So 1204501-41-6 is a valid CAS Registry Number.

1204501-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-c]pyridine

1.2 Other means of identification

Product number -
Other names 5-CHLORO-1-(PHENYLSULFONYL)-6-AZAINDOLE

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:1204501-41-6 SDS

1204501-41-6Relevant articles and documents

Heterocyclic compound as FGFR inhibitor, synthesis method and applications thereof

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, (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

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Paragraph 0147; 0191, (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.

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