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27471-40-5

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27471-40-5 Usage

Chemical structure

Piperidone derivative with a fluorine-substituted phenyl group

Potential applications

Pharmaceutical research and drug development

Structural features

Presence of a piperidone ring and a fluorine-substituted phenyl group

Biological activities

Unknown, but may be useful in targeting various biological pathways

Further research

Required to fully understand potential uses and effects in medicine and pharmacology

Check Digit Verification of cas no

The CAS Registry Mumber 27471-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,4,7 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27471-40:
(7*2)+(6*7)+(5*4)+(4*7)+(3*1)+(2*4)+(1*0)=115
115 % 10 = 5
So 27471-40-5 is a valid CAS Registry Number.

27471-40-5SDS

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 1-(4-fluorophenyl)piperidin-2-one

1.2 Other means of identification

Product number -
Other names 1-(4-FLUORO-PHENYL)-PIPERIDIN-2-ONE

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:27471-40-5 SDS

27471-40-5Relevant articles and documents

Discovery of novel c-met inhibitors bearing a 3-carboxyl piperidin-2-one scaffold

Zhang, Wei,Ai, Jing,Shi, Dakuo,Peng, Xia,Ji, Yinchun,Liu, Jian,Geng, Meiyu,Li, Yingxia

, p. 2655 - 2673 (2014/03/21)

A series of compounds containing a novel 3-carboxypiperidin-2-one scaffold based on the lead structure BMS-777607 were designed, synthesized and evaluated for their c-Met kinase inhibition and cytotoxicity against MKN45 cancer cell lines. The results indi

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