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3-benzylpiperidin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81976-72-9

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81976-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81976-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,9,7 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 81976-72:
(7*8)+(6*1)+(5*9)+(4*7)+(3*6)+(2*7)+(1*2)=169
169 % 10 = 9
So 81976-72-9 is a valid CAS Registry Number.

81976-72-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylmethyl-2-piperidinone

1.2 Other means of identification

Product number -
Other names 3-benzyl-2-piperidone

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:81976-72-9 SDS

81976-72-9Relevant articles and documents

One-pot oxidative Mannich-type reaction of lactams with alkyl malonates

Matsuo, Jun-ichi,Tanaki, Yumi,Ishibashi, Hiroyuki

, p. 3233 - 3236 (2008/02/02)

One-pot substitution of a C-H bond at the position next to the nitrogen atom of lactams with alkyl malonates proceeded effectively by dehydrogenation of lactams with N-tert-butylbenzenesulfinimidoyl chloride, followed by Mannich-type addition of alkyl malonates.

An aza-enolate alkylation strategy for the synthesis of α-alkyl-δ-amino esters and α-alkyl valerolactams

Taylor, Piers J. M.,Bull, Steven D.,Andrews, Philip C.

, p. 1347 - 1350 (2007/10/03)

Alkylation of the aza-enolate of valerolactim methyl ether with electrophiles affords α-alkyl lactims that may be hydrolysed under mild acidic conditions to afford their corresponding α-alkyl-δ-amino esters as their hydrochloride salts. Neutralisation of these salts with base results in smooth intramolecular cyclisation to afford their corresponding α-alkyl lactams in excellent yield. Georg Thieme Verlag Stuttgart.

Anticonvulsant and anxiolytic lactam and thiolactam derivatives

-

, (2008/06/13)

This invention relates to lactam and thiolactam derivatives having useful anticonvulsant and anxiolytic activity, pharmaceutical compositions containing these compounds and therapeutic applications using such compositions.

Piperidine derivatives

-

, (2008/06/13)

The invention provides piperidine derivatives of the general formula STR1 or an acid-addition salt or metal salt complex thereof, in which R represents a hydrogen atom or an optionally substituted alkyl, alkenyl, alkynyl, alkoxy, cycloalkyl, aryl, arylcarbonyl, heterocyclyl or heterocyclyloxy group; R1 represents an optionally substituted alkyl, phenyl, benzyl or cycloalkyl group; R2 represents a hydrogen atom or an optionally substituted alkyl group; one of W and X represents --CH2 --, --CH2 CH2 -- or --O--, the other of W and X being --CH2 -- or --CH2 CH2 or X represents a single chemical bond; m is 0 or 1 and n represents an integer from 0 to 3; processes for their preparation; compositions containing such compounds and their use as fungicides.

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