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3-Piperidinecarboxylic acid, 3-[(2-bromophenyl)methyl]-4-oxo-1-(phenylmethyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

929258-59-3

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929258-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 929258-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,2,5 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 929258-59:
(8*9)+(7*2)+(6*9)+(5*2)+(4*5)+(3*8)+(2*5)+(1*9)=213
213 % 10 = 3
So 929258-59-3 is a valid CAS Registry Number.

929258-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-benzyl-3-(2-bromobenzyl)-4-oxopiperidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl-3-(2-bromobenzyl)-N-benzyl-4-oxopiperidine-3-carboxylate

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:929258-59-3 SDS

929258-59-3Relevant academic research and scientific papers

Substituted tricyclic piperidone compounds

-

Page/Page column 5; 6, (2009/01/24)

Substituted tricyclic piperidone derivatives corresponding to Formula I: a method for producing such compounds; pharmaceutical compositions containing such compounds, and the use of such compounds to treat pain, depression, urinary incontinence, diarrhea, pruritus, alcohol and drug abuse, drug dependency, lethargy and/or anxiety.

Synthesis of benzomorphan analogues by intramolecular Buchwald-Hartwig cyclization

Khartulyari, Anton S.,Maier, Martin E.

, p. 317 - 324 (2007/10/03)

A new strategy toward the important class of benzomorphans is described. The key bond formation is based on an intramolecular Buchwald-Hartwig enolate arylation reaction. Thus, alkylation of piperidones with ortho-bromobenzyl bromides provides the necessary substrates. In the presence of a palladium catalyst, a sterically hindered phosphane ligand, and a base, carbon-carbon bond formation to tricyclic benzomorphan derivatives takes place. After removal of the N-protecting group, derivatization reactions are possible. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

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