Skip to Content
Merck
CN

36323

(S)-6-Oxo-2-piperidinecarboxylic acid

≥95.0% (HPLC)

Synonym(s):

6-Oxo-L-pipecolic acid, (S)-2-Piperidone-6-carboxylic acid, L-Pyrohomoglutamic acid

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C6H9NO3
CAS Number:
Molecular Weight:
143.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Assay:
≥95.0% (HPLC)
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

(S)-6-Oxo-2-piperidinecarboxylic acid, ≥95.0% (HPLC)

InChI

1S/C6H9NO3/c8-5-3-1-2-4(7-5)6(9)10/h4H,1-3H2,(H,7,8)(H,9,10)/t4-/m0/s1

SMILES string

OC(=O)[C@@H]1CCCC(=O)N1

InChI key

FZXCPFJMYOQZCA-BYPYZUCNSA-N

assay

≥95.0% (HPLC)

impurities

≤5.0% water

functional group

carboxylic acid

Quality Level

Application

(S)-6-Oxo-2-piperidinecarboxylic acid can be used as a reactant to synthesize:
  • Functionalized β-lactam N-heterocycles via carboxymethylproline synthase catalyzed cyclization reactions. Pro-(S)-C5 branched [4.3.1] aza-amide bicycles as potential inhibitors for FK506-binding proteins.
  • Ethyl (S)-2-(6-oxopiperidin-2-yl)acetate, which is reduced using LiBH4 to produce optically pure hydroxymethyl lactams.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Preparation of optically pure ω-hydroxymethyl lactams
Huang S-B, et al.
Synthetic Communications, 19(20), 3485-3496 (1989)
Rational Design and Asymmetric Synthesis of Potent and Neurotrophic Ligands for FK506-Binding Proteins (FKBPs)
Pomplun S, et al.
Angewandte Chemie (International ed. in English), 54(1), 345-348 (2015)
Carboxymethylproline synthase catalysed syntheses of functionalised N-heterocycles
Hamed RB, et al.
Chemical Communications (Cambridge, England), 46(9), 1413-1415 (2010)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service