3459-75-4

Basic information

• Product Name: N-cyclohexyl-N,N-dimethyl-methanimidamide
• CAS NO: 3459-75-4
• Molecular Formula: C₉H₁₈N₂
• Molecular Weight: 154.255
• Mol File: 3459-75-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-cyclohexyl-N,N-dimethyl-methanimidamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-cyclohexyl-N,N-dimethyl-methanimidamide(3459-75-4)
• EPA Substance Registry System: N-cyclohexyl-N,N-dimethyl-methanimidamide(3459-75-4)

Safety Data

• Hazardous Substances Data: 3459-75-4(Hazardous Substances Data)

Upstream product

• 108-91-8 cyclohexylamine 
• 68-12-2 N,N-dimethyl-formamide 
• 2214-88-2 Dimethylamino-aethoxy-acetonitril 
• 1122-82-3 isothiocyanatocyclohexane 
• 1178544-56-3 C₉H₁₈N₂O 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 
• 24070-58-4 N-cyclohexyl-N',N'-dimethylthiourea 

Downstream Products

• 81763-89-5 Cyclohexyl-[1-(3,4-dihydro-1H-isoquinolin-2-yl)-meth-(Z)-ylidene]-amine 
• 173737-57-0 2-<(cyclohexylimino)methyl>=1,2,3,4-tetrahydro-6,7-dimethoxyisoquinoline 
• 108-91-8 cyclohexylamine 
• 68-12-2 N,N-dimethyl-formamide 
• 81763-82-8 {2-[(E)-Cyclohexyliminomethyl]-1,2,3,4-tetrahydro-isoquinolin-1-yl}-(3,4-dimethoxy-phenyl)-methanol 
• 81763-81-7 Cyclohexyl-[1-[1-(3,4-dimethoxy-benzyl)-3,4-dihydro-1H-isoquinolin-2-yl]-meth-(E)-ylidene]-amine 
• 81763-78-2 [1-(1-Benzyl-3,4-dihydro-1H-isoquinolin-2-yl)-meth-(E)-ylidene]-cyclohexyl-amine 
• 81763-83-9 2-[(E)-Cyclohexyliminomethyl]-1,2,3,4-tetrahydro-isoquinoline-1-carboxylic acid ethyl ester 
• 75541-92-3 N-Butyl-N'-cyclohexyl-N-methyl-formamidine 
• 75541-93-4 N'-Cyclohexyl-N-isobutyl-N-methyl-formamidine 
• 1209-07-0 β-Cyclohexylamino-α-cyan-acrylsaeuremethylester 
• 46229-77-0 N'-Cyclohexyl-N,N-diethyl-formamidine 
• 75541-91-2 N'-Cyclohexyl-N-ethyl-N-methyl-formamidine 

Relevant articles and documents

Fast equilibrium of zwitterionic adduct formation in reversible fixation-release system of CO2 by amidines under dry conditions

We investigated the fixation of CO2 by several amidines in solution and found that simple monocyclic amidines fixed CO2 under dry conditions to quantitatively afford the corresponding bicarbonates through hydrolysis of the zwitterion

Synthetic potentiality of α-amino nitrones as oxidizing reagent in the conversion of alkyl halides to aldehydes

α-Amino nitrones have been used successfully as an oxidizing reagent for the synthesis of aldehydes from various alkyl halides with an excellent yield. In addition, hydrolysis of the side product (imines) furnishes starting material amides which are recyclable along with corresponding amines.

Amides and formamidines with antinociceptive activity (note II)

Forty amides, formamidines and trifluoromethylsulfonylamides bearing on the nitrogen a cyclohexyl residue, eventually 2-substituted, were prepared and tested for analgesic activity against a chemical stimulus. Good activity was exhibited by amides 9, 11 and 28, by formamidine 34, as well as by triflylamide 40. Eleven additional compounds exhibited a moderate activity.