31207-17-7

Basic information

• Product Name: 3-Buten-2-one, 3-bromo-4-phenyl-
• CAS NO: 31207-17-7
• Molecular Formula: C10H9BrO
• Molecular Weight: 225.085
• Mol File: 31207-17-7.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 3-Buten-2-one, 3-bromo-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Buten-2-one, 3-bromo-4-phenyl-(31207-17-7)
• EPA Substance Registry System: 3-Buten-2-one, 3-bromo-4-phenyl-(31207-17-7)

Safety Data

• Hazardous Substances Data: 31207-17-7(Hazardous Substances Data)

Upstream product

• 122-57-6 1-Phenylbut-1-en-3-one 
• 6310-44-7 3,4-dibromo-4-phenylbutan-2-one 
• 100-52-7 benzaldehyde 
• 127-09-3 sodium acetate 
• 34837-55-3 Phenylselenyl bromide 
• 344298-37-9 3-Bromo-4-hydroxy-4-phenyl-butan-2-one 
• 64-17-5 ethanol 
• 6310-44-7 rac-(R,S)-3,4-dibromo-4-phenylbutan-2-one 
• 98-86-2 acetophenone 

Downstream Products

• 800370-24-5 3-bromo-4-phenyl-4-piperidino-butan-2-one 
• 6283-29-0 3,4-dimorpholino-2,4-diphenyl-butan-2-ol 
• 5455-91-4 3,4-dimorpholino-4-phenylbutan-2-one 
• 56138-16-0 3-acetyl-2,5-diphenylfuran 
• 771477-49-7 (E)-3-benbenzylidene-5-phenylpent-4-yn-2-one 
• 1175095-52-9 (E)-3-benzylidene-5-(4-methoxyphenyl)pent-4-yn-2-one 
• 1021457-60-2 St_1e 
• 1172595-20-8 St_1f 
• 1382530-20-2 3-benzylidene-5-(4-bromophenyl)-4-pentyn-2-one 

Relevant articles and documents

Asymmetric Construction of 2,3-Dihydroisoxazoles via an Organocatalytic Formal [3 + 2] Cycloaddition of Enynes with N-Hydroxylamines

An organocatalytic asymmetric formal [3 + 2] cycloaddition of enynones with N-hydroxylamines has been described. A newly designed multifunctional organocatalyst was found to be highly effective, and the method allowed the synthesis of a variety of 2,3-dih

Dinucleophilic Reactivity of Isocyanoacetate: Base-Catalyzed One-Pot Access to 4-Azafluorenes and 4-Azafluorenones

A base-catalyzed double annulation of isocyanoacetates with various enynones has been developed for the expeditious synthesis of 4-azafluorene and 4-azafluorenone derivatives. Against the well-known 1,3-dipolar reactivities, the active methylene and isocy

Rapid assembly of 3-azidomethylfurans from 2-(1-alkynyl)-2-alken-1-ones enabled by silver catalysis

A rapid access to useful 3-azidomethylfurans is developed via Ag(I)-catalyzed cascade annulation/azidation of 2-(1-alkynyl)-2-alken-1-ones. The salient features of the protocol include mild reaction conditions, high efficiency, broad substrate scope, and