121129-35-9

Basic information

• Product Name: 2-Mandeloyl-3,6-dihydro-3,6-methano-2H-1,2-oxazine
• CAS NO: 121129-35-9
• Molecular Weight: 231.251
• Mol File: 121129-35-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Mandeloyl-3,6-dihydro-3,6-methano-2H-1,2-oxazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Mandeloyl-3,6-dihydro-3,6-methano-2H-1,2-oxazine(121129-35-9)
• EPA Substance Registry System: 2-Mandeloyl-3,6-dihydro-3,6-methano-2H-1,2-oxazine(121129-35-9)

Safety Data

• Hazardous Substances Data: 121129-35-9(Hazardous Substances Data)

Upstream product

• 126924-19-4 (2R)-(-)-2-hydroxy-2-phenylacetohydroxamic acid 
• 542-92-7 cyclopenta-1,3-diene 
• 4358-87-6 (RS)-methyl mandelate 
• 2292-53-7 (RS)-2-hydroxy-2-phenylacetohydroxamic acid 

Downstream Products

• 1110772-05-8 (1R,3S)-3-aminocyclopentan-1-ol 
• 1279032-31-3 (1R,3S)-3-amino-1-cyclopentanol hydrochloride 

Relevant articles and documents

Preparation method of (1R,3S)-3-amino-1-cyclopentanol and salt thereof

The invention discloses a preparation method of (1R,3S)-3-amino-1-cyclopentanol and a salt thereof, and relates to the field of organic synthesis. In the method, a chiral source in an N-Acyl hydroxylamine compound is used as chiral induction, and an asymm

ASYMMETRIC INDUCTION IN THE DIELS-ALDER REACTIONS OF α-HYDROXYACYLNITROSO COMPOUNDS

Transient, chiral α-hydroxyacylnitroso compounds (2), able to form intramolecular hydrogen bonds, react stereoselectively with cyclopentadiene and cyclohexa-1,3-diene; the cycloadduct (6) of the latter diene and the nitroso derivative of (S)-mandelic acid