135579-12-3

Basic information

• Product Name: Acetamide, N-3-buten-1-yl-N-phenyl-
• Synonyms: Acetamide, N-3-buten-1-yl-N-phenyl-
• CAS NO: 135579-12-3
• Molecular Formula: C₁₂H₁₅NO
• Molecular Weight: 189.25
• Mol File: 135579-12-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 280.7±19.0 °C(Predicted)
• Appearance: /
• Density: 1.019±0.06 g/cm3(Predicted)
• PKA: 0.49±0.50(Predicted)
• CAS DataBase Reference: Acetamide, N-3-buten-1-yl-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-3-buten-1-yl-N-phenyl-(135579-12-3)
• EPA Substance Registry System: Acetamide, N-3-buten-1-yl-N-phenyl-(135579-12-3)

Safety Data

• Hazardous Substances Data: 135579-12-3(Hazardous Substances Data)

Upstream product

• 135579-06-5 N-(2-bromophenyl)-N-but-3-enylacetamide 
• 222851-56-1 N-phenylsulfinylamine 
• 131196-24-2 2-phenyl-3,6-dihydro-2H-[1,2]thiazine 1-oxide 
• 17482-19-8 1-(but-3-en-1-ylsulfonyl)-4-methylbenzene 
• 103-84-4 Acetanilid 

Downstream Products

• 1064196-56-0 (E)-N-phenyl-N-(4-phenylbut-3-enyl)ethanamide 
• 1064196-53-7 methyl (E)-5-(N-phenylethanamido)pent-2-enoate 
• 70677-94-0 1,4-di(benzyloxy)but-2,3-ene 
• 1064196-55-9 (E)-N-phenyl-N-(4-(phenylsulfonyl)but-3-enyl)ethanamide 
• 1064196-54-8 tert-butyl (E)-5-(N-phenylethanamido)pent-2-enoate 
• 165276-60-8 (Z)-1,6-di(tert-butyldimethylsilyloxy)hex-3-ene 
• 240431-99-6 (E)-2,2,3,3,12,12,13,13-octamethyl-4,11-dioxa-3,12-disilatetradec-7-ene 
• 55385-49-4 6-(benzyloxy)hex-3-en-1-ol 

Relevant articles and documents

The formal [3+2+1] cyclisation of cyclopropylamines with carboxylic anhydrides: A quick access to polysubstituted 2,3,3a,4-tetrahydro-6(5H)-indolone ring systems

Several 2-azabicyclo[3.1.0]hexanes were synthesised using the intramolecular version of the Kulinkovich-de Meijere cyclopropanation reaction. Upon heating in the presence of a carboxylic anhydride, the cyclopropane rings of these systems open up to afford vinylogous amides. Depending on the reaction conditions used, the monoacylated compounds may be the major products, or subsequent acylation may take place to afford cyclic diketones. The method is flexible, and it is possible to incorporate different acyl groups in a two-step sequence. The diketones are easily converted into 2,3,3a,4-tetrahydro-6(5H)- indolone derivatives by intramolecular aldolisation. The products, which are highly functionalised alcohols, are obtained as single diastereoisomers. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.