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84619-48-7

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84619-48-7 Usage

General Description

2,5-piperidinedicarboxylic acid, also known as pipecolic acid, is a cyclic amino acid with the molecular formula C7H11NO4. It is a naturally occurring compound found in the human body and is also present in various plants and animals. Pipecolic acid plays a role in several biological processes, including the metabolism of lysine and the synthesis of neurotransmitters. It is also used in the synthesis of pharmaceuticals and agrochemicals. Additionally, pipecolic acid has been studied for its potential therapeutic effects in treating neurodegenerative diseases and inflammatory conditions. Overall, 2,5-piperidinedicarboxylic acid is a versatile compound with diverse biological and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 84619-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,6,1 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84619-48:
(7*8)+(6*4)+(5*6)+(4*1)+(3*9)+(2*4)+(1*8)=157
157 % 10 = 7
So 84619-48-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO4/c9-6(10)4-1-2-5(7(11)12)8-3-4/h4-5,8H,1-3H2,(H,9,10)(H,11,12)/t4-,5-/m0/s1

84619-48-7SDS

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 (2S,5S)-piperidine-2,5-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 2,5-Piperidinedicarboxylic acid,cis

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:84619-48-7 SDS

84619-48-7Relevant articles and documents

SYNTHESIS AND CONFIGURATION OF DIASTEREOMERIC 2,4-, 2,5-, AND 2,6-PIPERIDINEDICARBOXYLIC ACIDS AND THEIR DIMETHYL ESTERS

Mastafanova, L. I.,Turchin, K. F.,Evstratova, M. I.,Sheinker, Yu. N.,Yakhontov, L. N.

, p. 305 - 309 (2007/10/02)

The reduction in an acidic medium over a platinum catalysts of 2,4-, 2,5-, and 2,6-pyridinedicarboxylic acids gave cis-2,4-, -2,5-, and -2,6-piperidinedicarboxylic acids, heating of which in an alkaline medium led to thermodynamically equilibrium mixtures of diastereomers.Individual trans-2,5-piperidinecarboxylic acid was isolated.The configurations of the 2,4-, 2,5-, and 2,6-piperidinedicarboxylic acids and their methyl esters were established by means of the PMR spectra.

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