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Chemical structure of CAS 1723-00-8

Pipecolic acid, (+)-

In Stock•Starting at $7 for 1 g•Purity ≥ 97%
CAS No.1723-00-8
MDL No.MFCD00064346
MFC6H11NO2
MW129.16
InChI KeyHXEACLLIILLPRG-RXMQYKEDSA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
1 g97%$7In Stock
5 g97%$8In Stock
10 g97%$9In Stock
25 g97%$17In Stock
50 g97%$30In Stock
100 g97%$57In Stock
250 g97%$132In Stock
500 g97%$240In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

D-Pipecolic acid is the D-enantiomer of pipecolic acid. It functions as a human metabolite and is the conjugate acid of D-pipecolate. It is an enantiomer of L-pipecolic acid.

CAS No.1723-00-8
Product NamePipecolic acid, (+)-
IrritantIrritant
Signal Word:Warning
HCode:H315-H319-H335
PCode:P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

Related Articles

Studies related to this compound and its mechanism of action

Enantioselective allylation of imines catalyzed by newly developed (-)-β-pinene-based π-allylpalladium catalyst: an efficient synthesis of (R)-α-propylpiperonylamine and (R)-pipecolic acid.

Organic & biomolecular chemistry • Vol. 10, Issue 38 • 2012
PMID: 22910971DOI: 10.1039/c2ob26188j

An efficient synthesis of enantiomerically pure (R)-pipecolic acid, (S)-proline, and their N-alkylated derivatives.

The Journal of organic chemistry • Vol. 72, Issue 5 • 2007
PMID: 17256910DOI: 10.1021/jo062382i

[Regulation of the blood oxygen transport capacity in diabetes mellitus].

Fortschritte der Medizin • Vol. 94, Issue 10 • 1976
PMID: 9343

Documentation

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