101861-80-7

Basic information

• Product Name: N-hydroxy-4-propylcyclohexanimine
• Synonyms: N-hydroxy-4-propylcyclohexanimine
• CAS NO: 101861-80-7
• Molecular Weight: 155.24
• Mol File: 101861-80-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-hydroxy-4-propylcyclohexanimine(CAS DataBase Reference)
• NIST Chemistry Reference: N-hydroxy-4-propylcyclohexanimine(101861-80-7)
• EPA Substance Registry System: N-hydroxy-4-propylcyclohexanimine(101861-80-7)

Safety Data

• Hazardous Substances Data: 101861-80-7(Hazardous Substances Data)

Upstream product

• 1678-92-8 propylcyclohexane 
• 52204-65-6 4-n-propylcyclohexanol 
• 40649-36-3 4-propyl-cyclohexanone 

Downstream Products

• 102653-37-2 4-n-propylcyclohexylamine 
• 428481-22-5 (1r,4s)-4-propylcyclohexanamine 
• 428481-22-5 trans-4-propylcyclohexanamine 
• 315706-73-1 N-(4-propyl-cyclohexyl)-3-(3,4,5-trimethoxy-phenyl)-acrylamide 
• 315706-77-5 3-(2,4-dichloro-phenyl)-N-(4-propyl-cyclohexyl)-acrylamide 
• 315706-76-4 3-(4-bromo-phenyl)-N-(4-propyl-cyclohexyl)-acrylamide 
• 315706-75-3 3-(4-fluoro-phenyl)-N-(4-propyl-cyclohexyl)-acrylamide 
• 315706-72-0 4-nitro-N-(4-propyl-cyclohexyl)-benzamide 
• 315706-74-2 3-(4-chloro-phenyl)-N-(4-propyl-cyclohexyl)-acrylamide 
• 315706-81-1 morpholine-4-carboxylic acid (4-propyl-cyclohexyl)-amide 
• 315706-79-7 N-(4-propyl-cyclohexyl)-3-p-tolyl-acrylamide 
• 315706-68-4 4-bromo-N-(4-propyl-cyclohexyl)-benzamide 
• 315706-67-3 4-fluoro-N-(4-propyl-cyclohexyl)-benzamide 
• 315706-71-9 4-methyl-N-(4-propyl-cyclohexyl)-benzamide 

Relevant articles and documents

Synthesis of N-[4-(propyl)cyclohexyl]-amides with anti-inflammatory and analgesic activities

Seventeen (un)substituted N-[4-(propyl)cyclohexyl]-amides (6a-h, 7a-h and 8) were synthesized and tested as anti-inflammatory and analgesic agents. The substituents on the aromatic ring were chosen in order to study the influence of electron-withdrawing or electron-donating residues, that change the electronic density on the aromatic moiety. The pharmacological results allow drawing some preliminary considerations on structure-activity relationships. (C) 2000 Elsevier Science S.A.

Aliphatic C-H Bond Oxidation with Hydrogen Peroxide Catalyzed by Manganese Complexes: Directing Selectivity through Torsional Effects

Substituted N-cyclohexyl amides undergo aliphatic C-H bond oxidation with H2O2 catalyzed by manganese complexes. The reactions are directed by torsional effects leading to site-selective oxidation of cis-1,4-, trans-1,3-, and cis-1,2-cyclohexanediamides. The corresponding diastereoisomers are unreactive under the same conditions. Competitive oxidation of cis-trans mixtures of 4-substituted N-cyclohexylamides leads to quantitative conversion of the cis-isomers, allowing isolation and successive conversion of the trans-isomers into densely functionalized oxidation products with excellent site selectivity and good enantioselectivity.