10076-13-8

Basic information

• Product Name: Benzenamine,N,N'-methanetetraylbis[4-methoxy-
• Synonyms: Carbodiimide,bis(p-methoxyphenyl)- (6CI,7CI,8CI); Bis(4-methoxyphenyl)carbodiimide;Bis(p-methoxyphenyl)carbodiimide; Di-p-methoxyphenylcarbodiimide;N,N'-Bis(4-methoxyphenyl)carbodiimide; NSC 164989
• CAS NO: 10076-13-8
• Molecular Formula: C15H14 N2 O2
• Molecular Weight: 254.288
• Mol File: 10076-13-8.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzenamine,N,N'-methanetetraylbis[4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine,N,N'-methanetetraylbis[4-methoxy-(10076-13-8)
• EPA Substance Registry System: Benzenamine,N,N'-methanetetraylbis[4-methoxy-(10076-13-8)

Safety Data

• Hazardous Substances Data: 10076-13-8(Hazardous Substances Data)

Upstream product

• 5416-93-3 4-Methoxyphenyl isocyanate 
• 1227-45-8 1,3-bis-(p-methoxyphenyl)thiourea 
• 33904-05-1 2,2′-diisothiocyanato-1,1′-biphenyl 
• 14796-89-5 4-methoxy-N-(triphenylphosphoran-ylidene)-aniline 
• 726-42-1 di-p-tolylcarbodiimide 
• 104-94-9 4-methoxy-aniline 
• 2284-20-0 4-Methoxyphenyl isothiocyanate 
• 1227-44-7 N,N'-bis(4-methoxyphenyl)urea 
• 2101-87-3 p-methoxy-phenylazide 
• 1454-80-4 1,1'-biphenyl-2,2'-diamine 

Downstream Products

• 1152-75-6 N,N'-bis(4-methoxyphenyl)iminoformamide 
• 130214-84-5 2-[4-(4-Methoxy-phenyl)-3-(4-methoxy-phenylamino)-5-thioxo-4,5-dihydro-[1,2,4]triazol-1-yl]-N-phenyl-acetamide 
• 24807-27-0 1,3-bis(4-methoxyphenyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione 
• 1227-44-7 N,N'-bis(4-methoxyphenyl)urea 
• 454253-27-1 N-(4-methoxyphenyl)-N'-(4-methylphenyl)carbodiimide 
• 454253-24-8 C₅(CH₃)5Ir(NC₆H₄OCH₃)2CNC₆H₄OCH₃ 
• 726-42-1 di-p-tolylcarbodiimide 
• 196872-23-8 2,2-bis(trifluoromethyl)-4-(dimethyliminio)-1,3-bis(4-methoxyphenyl)-1,3-diaza-2-boratacyclobutane 
• 196871-99-5 1,1-bis(trifluoromethyl)-2-(4-methoxyphenyl)-7-methoxy-2,4-diaza-3-(dimethyliminio)-1-borata-1,2,3,4-tetrahydronaphthalene 

Relevant articles and documents

Synthesis of cyclic guanidines via Pd-catalyzed alkene carboamination

A new approach to the synthesis of substituted 5-membered cyclic guanidines is described. Palladium-catalyzed alkene carboamination reactions between acyclic N-allyl guanidines and aryl or alkenyl halides provide these products in good yield. This method

Manganese-catalyzed cleavage of a carbon-carbon single bond between carbonyl carbon and α-carbon atoms of ketones

Singled out: Treatment of ketones with carbodiimides in the presence of a catalytic amount of either [{HMn(CO)4}3] or [Mn 2(CO)10] gave amides in good to excellent yields. In this reaction, the carbon-carbon single bond of a ketone is cleaved efficiently. The reaction also proceeded by using isocyanates instead of carbodiimides. Copyright

Pushing back the limits of hydrosilylation: Unprecedented catalytic reduction of organic ureas to formamidines

Pushing back the limits: A novel catalytic transformation has been designed to prepare formamidine derivatives by reduction of substituted ureas with hydrosilanes. Simple iron catalysts based on commercially available iron salts and phosphine ligands prov