68843-68-5

Basic information

• Product Name: 1-phenyl-3-methyl-but-3-en-1-one oxime
• Synonyms: 1-phenyl-3-methyl-but-3-en-1-one oxime
• CAS NO: 68843-68-5
• Molecular Weight: 175.23
• Mol File: 68843-68-5.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: 1-phenyl-3-methyl-but-3-en-1-one oxime(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-3-methyl-but-3-en-1-one oxime(68843-68-5)
• EPA Substance Registry System: 1-phenyl-3-methyl-but-3-en-1-one oxime(68843-68-5)

Safety Data

• Hazardous Substances Data: 68843-68-5(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 52813-35-1 3-methyl-1-phenylbut-3-en-1-one 
• 23092-23-1 3-methyl-1-phenylbut-3-en-1-ol 
• 68843-62-9 5-(bromomethyl)-5-methyl-3-phenyl-4,5-dihydroisoxazole 

Downstream Products

• 55107-38-5 3-methyl-1-phenylbut-3-en-1-amine 
• 1221447-08-0 C₁₁H₁₃NO⁽¹⁸⁾O 
• 1221447-07-9 (5-methyl-3-phenyl-4,5-dihydroisoxazol-5-yl)methyl acetate 
• 77790-76-2 (5-methyl-3-phenyl-4,5-dihydroisoxazol-5-yl)methanol 
• 1403477-95-1 5-methyl-3-phenyl-5-((2,2,6,6-tetramethylpiperidin-1-yl)oxymethyl)-4,5-dihydroisoxazole 
• 117341-66-9 5-Methyl-3-phenyl-6H-[1,2]oxazine 
• 51067-05-1 5,5-dimethyl-3-phenyl-4,5-dihydroisoxazole 

Relevant articles and documents

Copper-catalyzed radical oxyallylation of olefins for the construction of alkene-containing isoxazolines

A radical-mediated approach to alkene oxyallylation using allylic oximes is described. The reaction proceeds under copper-catalytic redox-neutral conditions and tolerates various functional groups. This protocol thus enables the synthesis of structurally valuable isoxazolines and the introduction of a versatile olefin motif in a single step.

Enantioselective Synthesis of Isoxazolines Enabled by Palladium-Catalyzed Carboetherification of Alkenyl Oximes

Reported here is a highly efficient Pd/Xiang-Phos catalyzed enantioselective carboetherification of alkenyl oximes with either aryl or alkenyl halides, delivering various chiral 3,5-disubstituted and 3,5,5-trisubstituted isoxazolines in good yields with u

Copper-mediated oxysulfonylation of alkenyl oximes with sodium sulfinates: a facile synthesis of isoxazolines featuring a sulfone substituent

A novel and efficient Cu(OAc)2-mediated oxysulfonylation of alkenyl oximes with sodium sulfonates was developed. The reactions are easy to conduct, occur under mild conditions, and form a broad range of sulfone-substituted isoxazolines in good yields.