83196-21-8

Basic information

• Product Name: Urea, N-[(4-methoxyphenyl)methyl]-N'-phenyl-
• CAS NO: 83196-21-8
• Molecular Formula: C15H16N2O2
• Molecular Weight: 256.304
• Mol File: 83196-21-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Urea, N-[(4-methoxyphenyl)methyl]-N'-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Urea, N-[(4-methoxyphenyl)methyl]-N'-phenyl-(83196-21-8)
• EPA Substance Registry System: Urea, N-[(4-methoxyphenyl)methyl]-N'-phenyl-(83196-21-8)

Safety Data

• Hazardous Substances Data: 83196-21-8(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 83196-19-4 9,10-dihydro-N-(4-methoxyphenylacetyl)-9,10-dimethyl-9,10-epoxyiminoanthracene 
• 64-10-8 phenyl carbamate 
• 105-13-5 4-Methoxybenzyl alcohol 
• 501-82-6 N-phenylcarbamic acid 
• 2393-23-9 4-methoxy-benzylamine 
• 2594-06-1 2-(4-methoxyphenyl)acetohydroxamic acid 
• 103-71-9 phenyl isocyanate 
• 495-18-1 Benzohydroxamic acid 

Downstream Products

• 197635-71-5 N-phenyl-N-(4-methoxybenzyl)carbodiimide 

Relevant articles and documents

Synthesis method of substituted urea compound

The invention discloses a synthesis method of a substituted urea compound, which comprises the following steps: stirring aldehyde, N-aryl urea, trichlorosilane and Lewis base in an organic solvent ata temperature range of -20 DEG C to room temperature for

Parallel synthesis of ureas and carbamates from amines and CO2 under mild conditions

"Chemical Equation Presented" A mild and efficient library synthesis technique has been developed for the synthesis of ureas and carbamates from carbamic acids derived from the DBU-catalyzed reaction of amines and gaseous carbon dioxide. Carbamic acids derived from primary amines reacted with Mitsunobu reagents to generate isocyanates in situ which were condensed with primary and secondary amines to afford the desired ureas. Similarly, carbamic acids from secondary amines reacted with alcohols activated with Mitsunobu reagents to form carbamates.

Efficient Synthesis of Polysubstituted Acylguanidines and Guanylureas

(Benzotriazol-1-yl)carboximidamides were applied for the preparation of polysubstituted acylguanidines and guanylureas. The reaction sequence utilized mild conditions and gave high yields for final compounds and intermediates. The protocol developed allows for variation of the substituents at all positions of the products.