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210533-45-2

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210533-45-2 Usage

General Description

(S)-1-Benzyl-piperidine-2-carboxylic acid is a chemical compound that belongs to the class of piperidine derivatives. It is a chiral molecule with the (S) configuration around the piperidine ring. (S)-1-BENZYL-PIPERIDINE-2-CARBOXYLIC ACID has a benzyl group attached to the piperidine ring, and a carboxylic acid functional group at the 2 position. It is used as a building block in organic synthesis and can be used to prepare a variety of pharmaceutical and biologically active compounds. The presence of the piperidine ring and the carboxylic acid group gives this compound potential biological activity and it may have applications in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 210533-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,5,3 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 210533-45:
(8*2)+(7*1)+(6*0)+(5*5)+(4*3)+(3*3)+(2*4)+(1*5)=82
82 % 10 = 2
So 210533-45-2 is a valid CAS Registry Number.

210533-45-2SDS

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 (2S)-1-Benzyl-2-piperidinecarboxylic acid

1.2 Other means of identification

Product number -
Other names (-)-(2S)-1-benzylpiperidine-2-carboxylic acid

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:210533-45-2 SDS

210533-45-2Relevant articles and documents

Chemoenzymatic synthesis of (S)-2-cyanopiperidine, a key intermediate in the route to (S)-pipecolic acid and 2-substituted piperidine alkaloids

Nazabadioko, Serge,Perez, Ramon J.,Brieva, Rosario,Gotor, Vicente

, p. 1597 - 1604 (2007/10/03)

The preparation of (S)-2-cyanopiperidine 4 provides a new access to 2- substituted piperidines. This synthesis is based on an enantioselective (R)- oxynitrilase-catalyzed reaction for the preparation of (R)-(+)-6-bromo-2- hydroxyhexanenitrile 1 and the subsequent cyclization of this compound to yield the piperidine ring. The utilization of 4 as the starting material for the synthesis of (S)-2-aminomethylpiperidine 6, (R)-(-)-coniine 10 and (S)- (-)pipecolic acid 13 is also described.

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