838-98-2

Basic information

• Product Name: Benzenamine, N,N'-methanetetraylbis[4-chloro-
• CAS NO: 838-98-2
• Molecular Formula: C13H8Cl2N2
• Molecular Weight: 263.126
• Mol File: 838-98-2.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzenamine, N,N'-methanetetraylbis[4-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N,N'-methanetetraylbis[4-chloro-(838-98-2)
• EPA Substance Registry System: Benzenamine, N,N'-methanetetraylbis[4-chloro-(838-98-2)

Safety Data

• Hazardous Substances Data: 838-98-2(Hazardous Substances Data)

Upstream product

• 1220-00-4 1,3-bis(4-chlorophenyl)thiourea 
• 2131-55-7 4-Chlorophenyl isothiocyanate 
• 106-47-8 4-chloro-aniline 
• 1219-99-4 N,N'-bis(4-chlorophenyl)urea 
• 31641-65-3 N-p-chlorophenyltriphenylphosphinimine 
• 104-12-1 p-chlorphenylisocyanate 
• 932-98-9 1-chloro-4-nitroso-benzene 
• 160060-66-2 N,N'-Bis-(4-chloro-phenyl)-5H-4b,10,11-triaza-benzo[b]fluorene-10-carboxamidine 
• 75-15-0 carbon disulfide 
• 100398-76-3 N,N-bis-(4-chloro-phenyl)-thiourea 

Downstream Products

• 1261527-70-1 6-chloro-1-(p-chlorophenyl)-2-(piperidin-1-yl)-1H-benzo[d]imidazole 
• 1448523-77-0 (Z)-4-chloro-N-(3-(4-chlorophenyl)-1-isopropyl-4-phenylimidazolidin-2-ylidene)benzenamine 
• 57962-71-7 5-methyl-1-p-chlorophenyl-2-p-chlorophenylaminoimidazole 
• 95605-85-9 N,N'-Bis-(4-chloro-phenyl)-2-morpholin-4-yl-cyclohex-1-enecarboxamidine 
• 61387-07-3 3-(4-chloro-phenyl)-2-(4-chloro-phenylimino)-2,3,6,7-tetrahydro-5H-cyclopenta[e][1,3]oxazin-4-one 
• 16357-86-1 5-benzyl-6-chloro-3-(4-chloro-phenyl)-2-(4-chloro-phenylimino)-2,3-dihydro-[1,3]oxazin-4-one 
• 16357-87-2 6-chloro-3-(4-chloro-phenyl)-2-(4-chloro-phenylimino)-5-ethyl-2,3-dihydro-[1,3]oxazin-4-one 
• 16798-41-7 7-chloro-3-(4-chloro-phenyl)-2-(4-chloro-phenylimino)-2,3-dihydro-pyrano[3,4-e][1,3]oxazine-4,5-dione 
• 55425-14-4 3-(4-chloro-phenyl)-2-(4-chloro-phenylimino)-1,1-dioxo-1λ⁶-thiazolidin-4-one 
• 1219-99-4 N,N'-bis(4-chlorophenyl)urea 

Relevant articles and documents

A facile method for the preparation of carbodiimides from thioureas and (Boc)2O

A concise method for the preparation of carbodiimides from thioureas using di-tert-butyl dicarbonate [(Boc)2O] as the dehydrosulfurizative reagent has been developed. Using DMAP as the catalyst, a variety of symmetric and asymmetric 1,3-diaryl thioureas were converted into the corresponding carbodiimides efficiently in a short time.

"On water": Efficient iron-catalyzed cycloaddition of aziridines with heterocumulenes

In suspension: The reaction of aziridines with heterocumulenes in the presence of Fe(NO3)3×9 H2O in aqueous suspension provides access to functionalized five-membered heterocycles in good to high yields. This protocol has a wide substrate scope, is simple, and uses a nontoxic and cheap catalyst. Copyright

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