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137442-19-4

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137442-19-4 Usage

General Description

(R)-4-benzylpiperazine-2-carboxylic acid is a chemical compound that belongs to the class of piperazine derivatives. It is a chiral compound, meaning it has a non-superimposable mirror image. (R)-4-benzylpiperazine-2-carboxylic acid has been studied for its potential pharmacological properties, including its role as a potential ligand for certain receptors in the central nervous system. It is also being investigated for its potential use in drug design and development. The structure of (R)-4-benzylpiperazine-2-carboxylic acid makes it a promising candidate for further research in the field of medicinal chemistry and pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 137442-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,4 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137442-19:
(8*1)+(7*3)+(6*7)+(5*4)+(4*4)+(3*2)+(2*1)+(1*9)=124
124 % 10 = 4
So 137442-19-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O2/c15-12(16)11-9-14(7-6-13-11)8-10-4-2-1-3-5-10/h1-5,11,13H,6-9H2,(H,15,16)/t11-/m1/s1

137442-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-4-benzylpiperazine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names (R)-4-BENZYLPIPERAZINE-2-CARBOXYLICACID

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:137442-19-4 SDS

137442-19-4Upstream product

137442-19-4Relevant articles and documents

Enantiomerically pure 2-piperazinemethanols as novel chiral ligands of oxazaborolidine catalysts in enantioselective borane reductions

Inoue, Tsutomu,Sato, Daisuke,Komura, Kenichi,Itsuno, Shinichi

, p. 5379 - 5382 (1999)

Novel enantiomerically pure 2-piperazinemethanols (3-5) were synthesized from 2-piperazinecarboxylic acid 1. The asymmetric reduction of aromatic ketones, ketimine and oxime ether has been performed with reagents prepared from 2-piprazinemethanol and borane to yield enantiomerically enriched alcohols and amines, respectively. The preferred absolute configuration of the product was dependent on the structure of the sulfonyl substituent in the chiral ligand.

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