104937-84-0

Basic information

• Product Name: Benzenemethanamine, a-ethenyl-N-(4-methoxyphenyl)-
• CAS NO: 104937-84-0
• Molecular Formula: C16H17NO
• Molecular Weight: 239.317
• Mol File: 104937-84-0.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzenemethanamine, a-ethenyl-N-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanamine, a-ethenyl-N-(4-methoxyphenyl)-(104937-84-0)
• EPA Substance Registry System: Benzenemethanamine, a-ethenyl-N-(4-methoxyphenyl)-(104937-84-0)

Safety Data

• Hazardous Substances Data: 104937-84-0(Hazardous Substances Data)

Upstream product

• 917-57-7 vinyllithium 
• 783-08-4 [4-(benzylideneamino)phenyl]methanol 
• 1112-56-7 tetravinyltin (IV) 
• 138313-59-4 1-phenylallyl 2,2,2-trichloroacetimidate 
• 104-94-9 4-methoxy-aniline 
• 3536-96-7 vinylmagnesium chloride 
• 1613-90-7 4-methoxy-N-[(E)-phenylmethylidene]aniline 
• 69562-10-3 1-phenyl-3-phenylseleno-1-propene 

Downstream Products

• 1261161-53-8 1-(3-methoxy-phenyl)-3-(4-methoxy-phenyl)-1-methyl-3-((Z)-1-phenyl-propenyl)-urea 
• 1261161-47-0 1-(3-fluoro-phenyl)-3-(4-methoxy-phenyl)-1-methyl-3-((Z)-1-phenyl-propenyl)-urea 
• 1261161-64-1 (Z)-1-(4-methoxyphenyl)-3-methyl-1-(1-phenylprop-1-enyl)-3-(3-(trifluoromethyl)phenyl)urea 
• 1261161-50-5 (Z)-1-(2,6-dimethylphenyl)-3-(4-methoxyphenyl)-1-methyl-3-(1-phenylprop-1-enyl)urea 
• 1261161-55-0 (Z)-1-(4-methoxyphenyl)-3-methyl-1-(1-phenylprop-1-enyl)-3-(o-tolyl)urea 
• 1261161-59-4 (Z)-1-(4-methoxyphenyl)-3-methyl-1-(1-phenylprop-1-enyl)-3-(p-tolyl)urea 
• 1261161-66-3 1-(4-methoxy-phenyl)-3-methyl-3-phenyl-1-((Z)-1-phenyl-propenyl)-urea 
• 1261161-58-3 1-(4-chloro-phenyl)-3-(4-methoxy-phenyl)-1-methyl-3-((Z)-1-phenyl-propenyl)-urea 
• 1256930-07-0 1-(4-cyano-phenyl)-3-(4-methoxy-phenyl)-1-methyl-3-((Z)-1-phenyl-propenyl)-urea 
• 1256930-33-2 1-(4-cyanophenyl)-3-(4-methoxyphenyl)-1-methyl-3-(1-phenylallyl)urea 

Relevant articles and documents

Synthesis of 2-Alkenyl-Tethered Anilines

Three general routes for the synthesis of (E)-2-alkenyl-tethered anilines have been developed. The first route involves a 3-aza-Cope rearrangement of N -allylic anilines in the presence of a Lewis acid. The requisite N -allylic anilines were prepared by t

Aldehyde selective Wacker oxidations of phthalimide protected allylic amines: A new catalytic route to β3-amino acids

(Chemical Equation Presented) A new method for the synthesis of β3-amino acids is presented. Phthalimide protected allylic amines are oxidized under Wacker conditions selectively to aldehydes using PdCl2 and CuCl or Pd(MeCN)2/s

Enantioselective addition of organolithium reagents to imines mediated by c2-symmetric bis(aziridine) ligands

The C2-symmetric bis(aziridine) ligands 1-5 have been screened in the enantioselective addition of organolithium reagents to imines. Ligand 1 (used in stoichiometric amounts) was found to be superior in terms of chemical yield and enantioselect