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894767-26-1

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894767-26-1 Usage

General Description

(R)-4-oxopiperidine-2-carboxylic acid, also known as L-pipecolic acid, is a naturally occurring cyclic amino acid. It is a key intermediate in the biosynthesis of the non-protein amino acid, L-lysine, and is involved in the metabolism of the neurotransmitter, GABA. L-pipecolic acid has been found to have potential neuroprotective and anti-inflammatory properties, and has been studied for its potential therapeutic applications in treating neurodegenerative diseases and inflammatory conditions. It is also used as a precursor in the synthesis of pharmaceuticals and agrochemicals, making it a valuable chemical compound with diverse applications in research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 894767-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,4,7,6 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 894767-26:
(8*8)+(7*9)+(6*4)+(5*7)+(4*6)+(3*7)+(2*2)+(1*6)=241
241 % 10 = 1
So 894767-26-1 is a valid CAS Registry Number.

894767-26-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names -

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

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More Details:894767-26-1 SDS

894767-26-1Downstream Products

894767-26-1Relevant articles and documents

A new synthesis of (2S)-4-oxopipecolic acid by thermal rearrangement of enantiopure spirocyclopropaneisoxazolidine

Machetti, Fabrizio,Cordero, Franca M.,De Sarlo, Francesco,Guarna, Antonio,Brandi, Alberto

, p. 4205 - 4208 (2007/10/03)

A novel synthesis of (2S)-4-oxo-pipecolic acid is reported. The synthetic route employs as a key step the diastereoselective cycloaddition of the N- glycosylnitrone 7 to methylenecyclopropane followed by thermal rearrangement of the spirocyclopropaneisoxazolidine 8a. Stereoselective reduction of the N- BOC methyl ester of 4-oxopipecolic acid by L-selectride gives the protected cis-4-hydroxy-pipecolic acid 14.

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