17427-93-9

Basic information

• Product Name: Dodecanamide, N-cyclohexyl-
• CAS NO: 17427-93-9
• Molecular Formula: C18H35NO
• Molecular Weight: 281.482
• Mol File: 17427-93-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Dodecanamide, N-cyclohexyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Dodecanamide, N-cyclohexyl-(17427-93-9)
• EPA Substance Registry System: Dodecanamide, N-cyclohexyl-(17427-93-9)

Safety Data

• Hazardous Substances Data: 17427-93-9(Hazardous Substances Data)

Upstream product

• 143-07-7 lauric acid 
• 108-91-8 cyclohexylamine 
• 106-33-2 ethyl laurate 
• 1345092-81-0 C₁₅H₂₇O₃S^(1-)*Na⁽¹⁺⁾ 
• 112-16-3 n-dodecanoyl chloride 
• 111-82-0 methyl n-dodecanoate 

Downstream Products

• 78503-97-6 2-Chloro-4-phenyl-6-undecyl-[1,3,5]triazine 
• 124-22-1 n-Dodecylamine 
• 6490-87-5 N-dodecylcyclohexanamine 
• 108-91-8 cyclohexylamine 
• 101-83-7 N-cyclohexyl-cyclohexanamine 
• 80984-89-0 N-Cyclohexyl-dodecanimidoyl chloride; compound with GENERIC INORGANIC NEUTRAL COMPONENT 

Relevant articles and documents

Reaction of amphipathic-type thioester and amine with hydrophobic effect in water

The title reaction was studied using sodium 3-(1-oxododec-1-yl)thio- and 3-(1-oxohept-1-yl)thiopropanoate with various chain lengths of amines. The yields of the amides were found to depend on both the chain length of the thioester and that of amine, suggesting the presence of hydrophobic interaction. The amides were obtained in better yields after addition of sodium fluoride. Acylation (dodecanoylation) of some hydrophobic amino acids was also studied to obtain the corresponding amides. Georg Thieme Verlag Stuttgart - New York.

Antimony-templated macrolactamization of tetraamino esters. Facile synthesis of macrocyclic spermine alkaloids, (±)-buchnerine, (±)-verbacine, (±)-verbaskine, and (±)-verbascenine

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