Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

735566

Sigma-Aldrich

Ethyl (R)-1-Boc-4-oxopiperidine-2-carboxylate

97%

Synonym(s):

(R)-1-Boc-4-oxopiperidine-2-carboxylic acid ethyl ester

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C13H21NO5
CAS Number:
357154-16-6
Molecular Weight:
271.31
MDL number:
MFCD20526405
UNSPSC Code:
12352005
PubChem Substance ID:
329765035
NACRES:
NA.22

Assay

97%

form

solid

mp

42-47 °C

storage temp.

2-8°C

SMILES string

CCOC(=O)[C@H]1CC(=O)CCN1C(=O)OC(C)(C)C

InChI

1S/C13H21NO5/c1-5-18-11(16)10-8-9(15)6-7-14(10)12(17)19-13(2,3)4/h10H,5-8H2,1-4H3/t10-/m1/s1

InChI key

YAVQLRUBKDCOCI-SNVBAGLBSA-N

Related Categories

Application

Ethyl (R)-1-Boc-4-oxopiperidine-2-carboxylate can be used as a key intermediate in the preparation of 4-oxopipecolic acid enantiomer, a non-proteinogenic amino acid having antibiotic activity.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Precautionary Statements

P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Practical synthesis of both enantiomers of protected 4-oxopipecolic acid
Machetti F, et al.
Tetrahedron, 57(23), 4995-4998 (2001)

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