1251853-48-1

Basic information

• Product Name: 1-allyl-1-benzyl-3-phenylurea
• Synonyms: 1-allyl-1-benzyl-3-phenylurea
• CAS NO: 1251853-48-1
• Molecular Weight: 266.343
• Mol File: 1251853-48-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-allyl-1-benzyl-3-phenylurea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-allyl-1-benzyl-3-phenylurea(1251853-48-1)
• EPA Substance Registry System: 1-allyl-1-benzyl-3-phenylurea(1251853-48-1)

Safety Data

• Hazardous Substances Data: 1251853-48-1(Hazardous Substances Data)

Upstream product

• 33542-36-8 allyl(benzyl)carbamic chloride 
• 62-53-3 aniline 
• 4383-22-6 Allylbenzylamine 
• 100-52-7 benzaldehyde 
• 103-71-9 phenyl isocyanate 

Downstream Products

• 1251853-65-2 4-(azidomethyl)-1-benzyl-3-phenylimidazolidin-2-one 
• 1251853-61-8 1-benzyl-3-phenyl-4-((4-(trifluoromethyl)phenylamino)methyl)imidazolidin-2-one 
• 1251853-60-7 1-benzyl-4-((4-isopropylphenylamino)methyl)-3-phenylimidazolidin-2-one 
• 1251853-67-4 N-((1-benzyl-2-oxo-3-phenylimidazolidin-4-yl)methyl)benzamide 
• 1251853-64-1 1-benzyl-4-((3-methoxyphenylamino)methyl)-3-phenylimidazolidin-2-one 
• 1251853-59-4 1-benzyl-3-phenyl-4-((p-tolylamino)methyl)imidazolidin-2-one 
• 1251853-66-3 N-((1-benzyl-2-oxo-3-phenylimidazolidin-4-yl)methyl)-4-methylbenzenesulfonamide 
• 1251853-56-1 1-benzyl-3-phenyl-4-((phenylamino)methyl)imidazolidin-2-one 
• 1251853-90-3 1-benzyl-4-methyl-3-phenylimidazolidin-2-one 
• 1251853-62-9 1-benzyl-4-((2-chlorophenylamino)methyl)-3-phenylimidazolidin-2-one 
• 1455443-03-4 C₁₇H₁₇FN₂O 

Relevant articles and documents

Regioselective palladium-catalyzed intramolecular oxidative aminofluorination of unactivated alkenes

A novel Pd-catalyzed regioselective intramolecular aminofluorination of unactivated alkenes has been developed, which is an efficient method for the synthesis of a variety of monofluoromethylated nitrogen-containing heterocycles.

Copper-promoted and copper-catalyzed intermolecular alkene diamination

Simply copper: Copper(II)-promoted intra- and intermolecular olefin diaminations bring together two differently functionalized amines into a vicinal relationship. High diastereoselectivity was obtained with chiral alkenes and results of the asymmetric catalysis are promising. Copyright