2303-89-1

Basic information

• Product Name: Methanimidamide, N,N'-dicyclohexyl-
• CAS NO: 2303-89-1
• Molecular Formula: C13H24N2
• Molecular Weight: 208.347
• Mol File: 2303-89-1.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Methanimidamide, N,N'-dicyclohexyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanimidamide, N,N'-dicyclohexyl-(2303-89-1)
• EPA Substance Registry System: Methanimidamide, N,N'-dicyclohexyl-(2303-89-1)

Safety Data

• Hazardous Substances Data: 2303-89-1(Hazardous Substances Data)

Upstream product

• 290-87-9 1,3,5-Triazine 
• 108-91-8 cyclohexylamine 
• 97282-74-1 N-Dichlormethyl-N,N'-dicyclohexyl-formamidiniumchlorid 
• 74-90-8 hydrogen cyanide 
• 2387-23-7 1,3-Dicyclohexylurea 
• 538-75-0 dicyclohexyl-carbodiimide 
• 138996-50-6 C₃₂H₄₃N₃Si 
• 1212-29-9 1,3-dicyclohexylthiourea 
• 766-05-2 cyclohexane carbonitrile 
• 931-53-3 Cyclohexyl isocyanide 
• 124-38-9 carbon dioxide 
• 122-51-0 orthoformic acid triethyl ester 
• 14668-82-7 vinyl isocyanide 
• 53157-08-7 C₁₇H₃₄N₂Si 

Downstream Products

• 36739-76-1 6-(4-chloro-phenyl)-3-cyclohexyl-2-cyclohexylimino-2,3-dihydro-[1,3,5]oxadiazin-4-one 
• 36743-78-9 3-cyclohexyl-2-cyclohexylimino-6-(4-methoxy-phenyl)-2,3-dihydro-[1,3,5]oxadiazin-4-one 
• 36739-75-0 3-cyclohexyl-2-cyclohexylimino-6-phenyl-2,3-dihydro-[1,3,5]oxadiazin-4-one 
• 712349-49-0 N',N''-dicyclohexyl-N-furfuryl-guanidyno(ferrocenyl)methane phosphonous acid 
• 712349-47-8 N',N''-dicyclohexyl-N-benzyl-guanidyno(ferrocenyl)methanephosphonous acid 
• 906562-19-4 (N,N'-dicyclohexyl-N''-bis(trimethylsilyl)guanidinato)YCl₂(diethyl ether) 
• 1160709-85-2 (Nacnac)Mg{CyNC(H)NCy} 
• 1192370-99-2 Br^(1-)*C₁₆H₂₉N₂⁽¹⁺⁾ 
• 1472637-26-5 2,4-dicyclohexyl-4,5-dihydro-1H-benzo-1,3-diazepinium bromide 

Relevant articles and documents

Polynuclear Gold [AuI]4, [AuI]8, and Bimetallic [AuI4AgI] Complexes: C?H Functionalization of Carbonyl Compounds and Homogeneous Carbonylation of Amines

The synthesis of tetranuclear gold complexes, a structurally unprecedented octanuclear complex with a planar [AuI8] core, and pentanuclear [AuI4MI] (M=Cu, Ag) complexes is presented. The linear [AuI4] complex undergoes C?H functionalization of carbonyl compounds under mild reaction conditions. In addition, [AuI4AgI] catalyzes the carbonylation of primary amines to form ureas under homogeneous conditions with efficiencies higher than those achieved by gold nanoparticles.

Transfer hydrogenation promoted by N-heterocyclic carbene and water

N-Heterocyclic carbenes (NHCs) promote the transfer hydrogenation of various activated C=C, C=N, and N=N bonds with water as the proton source. The NHCs act as reducing reagents to be converted into their oxides. A detailed reaction mechanism is proposed on the basis of deuterium-labeling experiments.

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