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391344 Aldrich

(S)-(+)-2-Oxo-4-phenyl-3-oxazolidineacetic acid

98%

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Properties

Related Categories Asymmetric Synthesis, Chemical Synthesis, Chiral Auxiliaries, Oxazolidinone Derivatives
InChI Key   PUKMRNJLFMISMT-SECBINFHSA-N
assay   98%
optical activity   [α]28/D +165°, c = 2 in chloroform
mp   103-105 °C(lit.)

Description

Packaging

1 g in glass bottle

250 mg in glass bottle

Application

The chiral ketene derived from this product leads to chiral β-lactams via the Staudinger reaction. This strategy has been extended to prepare unnatural dipeptides.

Price and Availability

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles
Peer-Reviewed Papers
15

References

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