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27471-52-9

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27471-52-9 Usage

Chemical structure

A piperidinone derivative with a trifluoromethyl phenyl group attached to the piperidine ring

Field of application

Medicinal chemistry and pharmaceutical research

Role

Building block for the synthesis of various biologically active compounds

Unique properties

Valuable tool in the development of new drugs and potential therapeutic agents

Potential applications

Agrochemicals and materials science industries

Further research

Needed to fully explore and understand the potential uses and properties of the compound

Check Digit Verification of cas no

The CAS Registry Mumber 27471-52-9 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, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 27471-52:
(7*2)+(6*7)+(5*4)+(4*7)+(3*1)+(2*5)+(1*2)=119
119 % 10 = 9
So 27471-52-9 is a valid CAS Registry Number.

27471-52-9SDS

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-(trifluoromethyl)phenyl]piperidin-2-one

1.2 Other means of identification

Product number -
Other names HMS1439F18

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:27471-52-9 SDS

27471-52-9Relevant articles and documents

Ruthenium-Pincer-Catalyzed Hydrogenation of Lactams to Amino Alcohols

Chen, Jiangbo,Wang, Jiaquan,Tu, Tao

, p. 2559 - 2565 (2018/07/30)

By using the commercially available ruthenium pincer complex (Ru-MACHO-BH) as a catalyst, the challenging direct hydrogenation of lactams and analogues has been successfully accomplished to deliver corresponding value-added amino alcohols in good-to-excellent yields under mild reaction conditions. Remarkably, in addition to N-protected lactams, unprotected ones could also be readily reduced in the presence of a catalytic amount of weak base or even under neutral reaction conditions, which further highlights the broad substrate scope and the protocol efficiency.

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