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911298-12-9

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911298-12-9 Usage

General Description

N-1-CBZ-2-Trifluoromethyl piperidin-4-one is a chemical compound that is used in pharmaceutical research and development as a building block for the synthesis of various drug molecules. It is a piperidinone derivative that contains a trifluoromethyl group and a carbobenzyloxy (Cbz) protecting group. The compound has potential applications in the synthesis of drugs for conditions such as cancer, neurological disorders, and infectious diseases. It is also used as a reagent in organic chemistry for the formation of various heterocyclic compounds. N-1-CBZ-2-Trifluoromethyl piperidin-4-one is a valuable intermediate in the production of pharmaceuticals and has potential for further exploration in drug discovery and drug design.

Check Digit Verification of cas no

The CAS Registry Mumber 911298-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,2,9 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 911298-12:
(8*9)+(7*1)+(6*1)+(5*2)+(4*9)+(3*8)+(2*1)+(1*2)=159
159 % 10 = 9
So 911298-12-9 is a valid CAS Registry Number.

911298-12-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 4-oxo-2-(trifluoromethyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names (+/-)-N-(benzyloxycarbonyl)-2-(trifluoromethyl)piperidin-4-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:911298-12-9 SDS

911298-12-9Relevant articles and documents

A simple stereoselective route to α-trifluoromethyl analogues of piperidine alkaloids

Bariau, Annabelle,Jatoi, Wahid Bux,Calinaud, Pierre,Troin, Yves,Canet, Jean-Louis

, p. 3421 - 3433 (2007/10/03)

The highly diastereoselective synthesis of five trifluoro-substituted analogues of mono-, di-, and trisubstituted piperidine alkaloids was accomplished in two to four steps from 2-trifluoromethyl keto-protected 4-piperidones, prepared by an intramolecular

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