53693-57-5

Basic information

• Product Name: Urea, N'-phenyl-N,N-bis(phenylmethyl)-
• Synonyms: N,N-Dibenzyl-N'-phenyl-harnstoff;N,N-dibenzyl-N'-phenylurea;N'-phenyl-N,N-bis(phenylmethyl)urea;1,1-Dibenzyl-3-phenylharnstoff
• CAS NO: 53693-57-5
• Molecular Formula: C21H20N2O
• Molecular Weight: 316.403
• Mol File: 53693-57-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Urea, N'-phenyl-N,N-bis(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Urea, N'-phenyl-N,N-bis(phenylmethyl)-(53693-57-5)
• EPA Substance Registry System: Urea, N'-phenyl-N,N-bis(phenylmethyl)-(53693-57-5)

Safety Data

• Hazardous Substances Data: 53693-57-5(Hazardous Substances Data)

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 103-49-1 dibenzylamine 
• 103-70-8 Formanilid 
• 64-10-8 phenyl carbamate 
• 102-07-8 bis(diphenyl)urea 
• 3422-02-4 N-(benzyloxycarbonyl)aniline 
• 25370-09-6 dibenzylcarbamyl chloride 
• 62-53-3 aniline 
• 103-71-9 phenyl isocyanate 

Downstream Products

• 103-49-1 dibenzylamine 
• 130935-33-0 4-acetyl-5-carbmethoxy-1-(dibenzylamino)-6H-7-oxa-3-oxo-2-phenyl-2-azabicyclo<2.2.1>hept-5-ene 
• 130935-32-9 4-acetyl-6-carbomethoxy-1-(dibenzylamino)-5H-7-oxa-3-oxo-2-phenyl-2-azabicyclo<2.2.1>hept-5-ene 
• 130935-30-7 N'-(diazoacetoacetyl)-N'-phenyl-N,N-bis(phenylmethyl)urea 
• 102-07-8 bis(diphenyl)urea 
• 130935-37-4 N'-acetoacetyl-N'-phenyl-N,N-bis(phenylmethyl)urea 

Relevant articles and documents

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Synthesis of unsymmetrical phenylurea derivatives via oxidative cross coupling of aryl formamides with amines under metal-free conditions

A new synthetic approach for phenylurea derivatives involving the cross coupling of N-aryl formamides with amines through the formation of isocyanate intermediates in the presence of hypervalent iodine reagents is described.

An efficient and mild protocol for the synthesis of unsymmetrical ureas in the absence of catalyst and additives

A new practical method for the synthesis of unsymmetrical ureas was achieved by reaction of phenylurea with primary and secondary amines under neutral and mild condition in very good yields. The reaction took place in refluxing dioxane and does not require any catalyst or additives.