1403477-87-1

Basic information

• Product Name: (E)-cyclohex-2-en-1-yl(phenyl)methanone oxime
• Synonyms: (E)-cyclohex-2-en-1-yl(phenyl)methanone oxime
• CAS NO: 1403477-87-1
• Molecular Weight: 201.268
• Mol File: 1403477-87-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-cyclohex-2-en-1-yl(phenyl)methanone oxime(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-cyclohex-2-en-1-yl(phenyl)methanone oxime(1403477-87-1)
• EPA Substance Registry System: (E)-cyclohex-2-en-1-yl(phenyl)methanone oxime(1403477-87-1)

Safety Data

• Hazardous Substances Data: 1403477-87-1(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 87938-65-6 1-phenyl-1-(3-cyclohex-1-enyl)-methanol 
• 1521-51-3 rac-3-bromocyclohexene 
• 29373-01-1 cyclohex-2-en-1-yl(phenyl)methanone 

Relevant articles and documents

Green organocatalytic synthesis of isoxazolines via a one-pot oxidation of allyloximes

A green, sustainable, organocatalytic, and efficient synthesis of isoxazolines from allyloximes was developed. A 2,2,2-trifluoroacetophenone-catalyzed oxidation of allyloximes, utilizing H2O2 as the green oxidant, was taken advantage of in order to introduce a cheap and environmentally friendly protocol for the synthesis of substituted isoxazolines. A variety of substitution patterns, both aromatic and aliphatic moieties, are well tolerated, leading to isoxazolines in moderate to excellent yields.

Copper-catalyzed oxyazidation of unactivated alkenes: A facile synthesis of isoxazolines featuring an azido substituent

A novel and efficient Cu(OAc)2-catalyzed oxyazidation of unactivated alkenes was developed. The reactions are easy to conduct, occur under mild conditions, and form azido-substituted isoxazolines in good yields.