laevo-pipecolinic acid
(S)-piperidine-2-carboxylic acid
Identification
| Name | laevo-pipecolinic acid |
| CAS Number | 3105-95-1 |
| EINECS | 221-462-1 |
| FDA UNII | 69374CKB33 |
| Molecular Formula | C6 H11 N O2 |
| Molecular Weight | 129.15907000 |
| MDL Number | MFCD00005981 |
| Nikkaji Number | J215.717I |
| Beilstein | 81093 |
| XlogP3 | -2.30 (est) |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 7.406e+004 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for laevo-pipecolinic acid usage levels up to | not for fragrance use. |
| Recommendation for laevo-pipecolinic acid flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
Synonyms
pipecolic acid, (-)-
L-
pipecolinic acid
(2S)-
piperidine-2-carboxylic acid
(S)-
piperidine-2-carboxylic acid
2-
piperidinecarboxylic acid, (S)- (9CI)
PubMed:
Xylapeptide A, an Antibacterial Cyclopentapeptide with an Uncommon L-Pipecolinic Acid Moiety from the Associated Fungus Xylaria sp. (GDG-102).
PubMed:
Regio- and stereoselective oxygenation of proline derivatives by using microbial 2-oxoglutarate-dependent dioxygenases.
PubMed:
Identification and characterization of 2-oxoglutarate-dependent dioxygenases catalyzing selective cis-hydroxylation of proline and pipecolinic acid from actinomycetes.
PubMed:
L-Pipecolinic acid derived Lewis base organocatalyst for asymmetric reduction of N-aryl imines by trichlorosilane: effects of the side amide group on catalytic performances.
PubMed:
A water-soluble calix[4]resorcinarene with L-pipecolinic acid groups as a chiral NMR solvating agent.
PubMed:
Synthesis of function-oriented 2-phenyl-2H-chromene derivatives using L-pipecolinic acid and substituted guanidine organocatalysts.
PubMed:
Evolution of chiral Lewis basic N-formamide as highly effective organocatalyst for asymmetric reduction of both ketones and ketimines with an unprecedented substrate scope.
PubMed:
Sequencing and analysis of the biosynthetic gene cluster of the lipopeptide antibiotic Friulimicin in Actinoplanes friuliensis.
PubMed:
A highly enantioselective lewis basic organocatalyst for reduction of N-aryl imines with unprecedented substrate spectrum.
PubMed:
Petrosifungins A and B, novel cyclodepsipeptides from a sponge-derived strain of Penicillium brevicompactum.
PubMed:
Synthesis and structure-activity relationships of gelatinase inhibitors derived from matlystatins.
PubMed:
The isolation of L-pipecolinic acid from Trifolium repens.
PubMed:
Naturally occurring L-pipecolinic acid.