1246285-32-4

Basic information

• Product Name: (2S,3S,4S)-2,3-epoxy-4-hexanoyloxy-5-[(2-hexanoyloxybenzoyl)amino]cyclohex-5-en-1-one
• Synonyms: (2S,3S,4S)-2,3-epoxy-4-hexanoyloxy-5-[(2-hexanoyloxybenzoyl)amino]cyclohex-5-en-1-one
• CAS NO: 1246285-32-4
• Molecular Weight: 457.524
• Mol File: 1246285-32-4.mol

Chemical Properties

• CAS DataBase Reference: (2S,3S,4S)-2,3-epoxy-4-hexanoyloxy-5-[(2-hexanoyloxybenzoyl)amino]cyclohex-5-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S,4S)-2,3-epoxy-4-hexanoyloxy-5-[(2-hexanoyloxybenzoyl)amino]cyclohex-5-en-1-one(1246285-32-4)
• EPA Substance Registry System: (2S,3S,4S)-2,3-epoxy-4-hexanoyloxy-5-[(2-hexanoyloxybenzoyl)amino]cyclohex-5-en-1-one(1246285-32-4)

Safety Data

• Hazardous Substances Data: 1246285-32-4(Hazardous Substances Data)

Upstream product

• 2051-49-2 n-hexanoic anhydride 
• 287194-40-5 (-)-2-hydroxy-N-(2-hydroxy-5-oxo-7-oxabicyclo[4.1.0]hept-3-en-3-yl)benzamide 

Relevant articles and documents

Chemoenzymatic synthesis of (2S,3S,4S)-form, the physiologically active stereoisomer of dehydroxymethylepoxyquinomicin (DHMEQ), a potent inhibitor on NF-κB

A new route for (2S,3S,4S)-form, the physiologically active stereoisomer of dehydroxymethylepoxyquinomicin (DHMEQ), a potent NF-κB inhibitor, was established by chemoenzymatic approach. Elaboration on the asymmetric epoxidation of a p-benzoquinone monoket