6951-34-4

Basic information

• Product Name: 5-(cyclohexylamino)pentan-1-ol
• CAS NO: 6951-34-4
• Molecular Formula: C₁₁H₂₃NO
• Molecular Weight: 185.3064
• Mol File: 6951-34-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 297.6°C at 760 mmHg
• Flash Point: 90°C
• Density: 0.93g/cm³
• Vapor Pressure: 0.000135mmHg at 25°C
• Refractive Index: 1.479
• CAS DataBase Reference: 5-(cyclohexylamino)pentan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(cyclohexylamino)pentan-1-ol(6951-34-4)
• EPA Substance Registry System: 5-(cyclohexylamino)pentan-1-ol(6951-34-4)

Safety Data

• Hazardous Substances Data: 6951-34-4(Hazardous Substances Data)

Upstream product

• 2622-52-8 cyclohexyl-tetrahydropyran-2-yl-amine 
• 4221-03-8 5-hydroxypentanal 
• 108-91-8 cyclohexylamine 
• 100400-10-0 cyclohexyl-tetrahydropyran-2-ylidene-amine 
• 2508-29-4 5-hydroxypentylamine 
• 108-94-1 cyclohexanone 
• 694-54-2 tetrahydro-2H-2-pyranol 
• 5259-98-3 5-chloropentan-1-ol 

Downstream Products

• 105695-20-3 N-Cyclohexyl-4-(3-formyl-4-nitro-phenoxy)-N-(5-hydroxy-pentyl)-butyramide 
• 77160-82-8 5-(1-Phenyl-cyclohexylamino)-pentan-1-ol 
• 105695-34-9 N-Cyclohexyl-N-(5-hydroxy-pentyl)-4-(2-oxo-1,2,3,5-tetrahydro-imidazo[2,1-b]quinazolin-7-yloxy)-butyramide 
• 77160-83-9 5-pentanoic acid 
• 77160-80-6 methyl 5-pentanoate 

Relevant articles and documents

Mammalian metabolism of phencyclidine

In dogs, the major metabolite of phencyclidine was found to be 5-[N-(1'-phenylcyclohexyl) amino]pentanoic acid (1). The γ-aminobutyric acid like metabolite was also pharmacologically evaluated to determine if the purported GABA-ergic mediated effects of p

Indirect monoalkylation of primary and secondary amines by reductive decyanation of α-aminonitriles with sodium cyanoborohydride-mercury bis(trifluoroacetate)

Secondary and tertiary amines are prepared from α-aminonitriles by selective reductive cleavage of the cyanide moiety. The α-aminonitriles in this case, function as 'masked' imine or iminium ions and are 'unmasked' by mercury(II) in the presence of sodium cyanoborohydride to obtain the reduced product. Secondary amines may be prepared indirectly from primary amines in good yield without danger of over alkylation.