Skip to Content
MilliporeSigma
All Photos(1)

Documents

473278

Sigma-Aldrich

(S)-(−)-4-Oxo-2-azetidinecarboxylic acid

98%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C4H5NO3
CAS Number:
Molecular Weight:
115.09
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

optical activity

[α]20/D −46°, c = 1 in methanol

mp

99-102 °C (lit.)

SMILES string

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

InChI

1S/C4H5NO3/c6-3-1-2(5-3)4(7)8/h2H,1H2,(H,5,6)(H,7,8)/t2-/m0/s1

InChI key

YSPMLLKKKHCTBN-REOHCLBHSA-N

General description

The crystals of (S)-(-)-4-oxo-2-azetidinecarboxylic acid are orthorhombic and belongs to P212121 space group.

Application

Important building block for the synthesis of NMDA receptor antagonists, 3-alkyl-L-aspartic acids, and orally active β-lactam inhibitors.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

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

Structures of (S)-(-)-4-oxo-2-azetidinecarboxylic acid and 3-azetidinecarboxylic acid from powder synchrotron diffraction data.
Mora AJ, et al.
Acta Crystallographica Section B, Structural Science, Crystal Engineering and Materials, 62(4), 606-611 (2006)
Hanessian, S. et al.
Synlett, 33-33 (1992)
Baldwin, J.E. et al.
Tetrahedron, 51, 11581-11581 (1995)
P E Finke et al.
Journal of medicinal chemistry, 38(13), 2449-2462 (1995-06-23)
The stereospecific synthesis of several 4-[(4-carboxyphenyl)oxy]- 3,3-dialkyl-1-[[(1-phenylalkyl)-amino]carbonyl]azetidin-2-on es 3 is described in which the C-3 alkyl groups were varied from methyl to butyl as well as allyl, benzyl and methoxymethyl. The structure-activity relations for these compounds are discussed in terms

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