1399841-11-2

Basic information

• Product Name: (1S,4R,5S)-ethyl 5-([1,1'-biphenyl]-4-yl)-7-oxo-6-oxabicyclo[3.2.0]heptane-4-carboxylate
• Synonyms: (1S,4R,5S)-ethyl 5-([1,1'-biphenyl]-4-yl)-7-oxo-6-oxabicyclo[3.2.0]heptane-4-carboxylate
• CAS NO: 1399841-11-2
• Molecular Weight: 336.387
• Mol File: 1399841-11-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,4R,5S)-ethyl 5-([1,1'-biphenyl]-4-yl)-7-oxo-6-oxabicyclo[3.2.0]heptane-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,4R,5S)-ethyl 5-([1,1'-biphenyl]-4-yl)-7-oxo-6-oxabicyclo[3.2.0]heptane-4-carboxylate(1399841-11-2)
• EPA Substance Registry System: (1S,4R,5S)-ethyl 5-([1,1'-biphenyl]-4-yl)-7-oxo-6-oxabicyclo[3.2.0]heptane-4-carboxylate(1399841-11-2)

Safety Data

• Hazardous Substances Data: 1399841-11-2(Hazardous Substances Data)

Upstream product

• 57477-98-2 3-biphenyl-4-yl-3-oxopropionic acid ethyl ester 
• 1399840-71-1 (E)-ethyl 2-([1,1'-biphenyl]-4-carbonyl)-6-hydroxyhex-4-enoate 
• 1399840-94-8 (E)-ethyl 2-([1,1'-biphenyl]-4-carbonyl)-6-oxohex-4-enoate 

Relevant articles and documents

Catalytic dynamic kinetic resolutions with N-heterocyclic carbenes: Asymmetric synthesis of highly substituted β-lactones

New DKR type: An N-heterocyclic carbene (NHC)-catalyzed dynamic kinetic resolution of racemic α-substituted β-keto esters has been developed. This method relies on the epimerization of an NHC-enol intermediate before subsequent aldol/acylation events. Hig