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D-Pipecolic Acid

CAT: 0127-OR350111-01Size: 25 gDry Ice: NoHazardous: No
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CAS Number
1723-00-8
Synonyms
(R) -Piperidine-2-carboxylic acid, D-Homoproline
MDL Number
MFCD00064346
Purity
98%
Smiles
OC(=O)[C@H]1CCCCN1

Chemical Information

Pipecolic acid, (+)-

D-pipecolic acid is the D-enantiomer of pipecolic acid. It has a role as a human metabolite. It is a conjugate acid of a D-pipecolate. It is an enantiomer of a L-pipecolic acid.

CAS Number1723-00-8
PubChem CID736316
IUPAC Name(2R)-piperidine-2-carboxylic acid
Molecular FormulaC6H11NO2
Molecular Weight129.16
XLogP-2.3
Topological Polar Surface Area49.3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Heavy Atom Count9
Formal Charge0
Complexity114
SMILES
C1CCN[C@H](C1)C(=O)O
InChI
InChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m1/s1
InChIKey
HXEACLLIILLPRG-RXMQYKEDSA-N
Chemical Structure
2D Structure
2D structure of Pipecolic acid, (+)-
CAS: 1723-00-8
CID: 736316
Formula: C6H11NO2
MW: 129.16
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight129.16
XLogP3-2.3
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass129.078978594
Monoisotopic Mass129.078978594
Topological Polar Surface Area49.3 Ų
Heavy Atom Count9
Formal Charge0
Complexity114
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes