1024596-39-1

Basic information

• Product Name: 1-phenyl-7-methyloct-6-en-3-one oxime
• Synonyms: 1-phenyl-7-methyloct-6-en-3-one oxime
• CAS NO: 1024596-39-1
• Molecular Weight: 231.338
• Mol File: 1024596-39-1.mol

Chemical Properties

• CAS DataBase Reference: 1-phenyl-7-methyloct-6-en-3-one oxime(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-7-methyloct-6-en-3-one oxime(1024596-39-1)
• EPA Substance Registry System: 1-phenyl-7-methyloct-6-en-3-one oxime(1024596-39-1)

Safety Data

• Hazardous Substances Data: 1024596-39-1(Hazardous Substances Data)

Upstream product

• 35519-96-1 7-methyl-1-phenyloct-6-en-3-one 
• 645-45-4 hydrocinnamic acid chloride 
• 170646-96-5 N-methoxy-N-methyl-3-phenylpropionamide 

Downstream Products

• 1024596-46-0 7,7-dimethyl-3-(2-phenylethyl)-4,5,6,7-tetrahydro-1,2-oxazepine 
• 35519-96-1 7-methyl-1-phenyloct-6-en-3-one 
• 628691-81-6 7-methyl-1-phenyl-6-octen-3-one O-acetyloxime 
• 646039-23-8 1-phenyl-7-methyloct-6-en-3-one O-methoxyacetyloxime 

Relevant articles and documents

Synthesis of Quinolines and 2H-Dihydropyrroles by Nucleophilic Substitution at the Nitrogen Atom of Oxime Derivatives

Isomerization of oxime derivatives was researched in detail to find out the methods for the syn-anti isomerization of O-substituted oximes. Based on these findings were developed simple methods for the preparation of aza-heterocycles from both stereoisomers of oximes. Quinolines were synthesized from β-aryl ketone oximes by treatment with trifluoroacetic anhydride and 4-chloranil. γ,δ-Unsaturated O-methoxyacetyloximes were transformed to 2H-dihydropyrroles by reaction with methoxy-acetic acid.