N-Cyclohexyloctanamide

Base Information

• Chemical Name: N-Cyclohexyloctanamide
• CAS No.: 42577-04-8
• Molecular Formula: C14H27 N O
• Molecular Weight: 225.374
• Hs Code.: 2924299090
• European Community (EC) Number: 255-895-2
• DSSTox Substance ID: DTXSID70195356
• Nikkaji Number: J309.952K
• Wikidata: Q83068257
• Mol file: 42577-04-8.mol

Synonyms:N-Cyclohexyloctanamide;42577-04-8;EINECS 255-895-2;MLS006026925;SCHEMBL14520558;DTXSID70195356;AKOS003479955;SMR004718316

Chemical Property of N-Cyclohexyloctanamide

Chemical Property:

• Vapor Pressure: 8.09E-06mmHg at 25°C
• Boiling Point: 374.9°Cat760mmHg
• Flash Point: 228.2°C
• PSA: 32.59000
• Density: 0.91g/cm³
• LogP: 4.63610
• XLogP3: 4.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 7
• Exact Mass: 225.209264485
• Heavy Atom Count: 16
• Complexity: 185

Purity/Quality:

99% ^*data from raw suppliers

N-CYCLOHEXYLOCTANAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CCCCCCCC(=O)NC1CCCCC1

Technology Process of N-Cyclohexyloctanamide

There total 9 articles about N-Cyclohexyloctanamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

octanoic acid ethyl ester (106-32-1) + cyclohexylamine (108-91-8,157973-60-9) → N-(cyclohexyl)-n-octanoylamide (42577-04-8)

Guidance literature:

With potassium tert-butylate; for 0.0583333h; microwave irradiation;

Reference yield: 86.0%

1-bromocyclohexane (108-85-0) + n-octanamide (629-01-6) → N-(cyclohexyl)-n-octanoylamide (42577-04-8)

Guidance literature:

1-bromocyclohexane; n-octanamide; With copper(l) iodide; lithium tert-butoxide; In N,N-dimethyl-formamide; acetonitrile; at 20 ℃; for 0.0833333h; Inert atmosphere;

In N,N-dimethyl-formamide; acetonitrile; at 20 ℃; for 24h; Inert atmosphere; Irradiation;

DOI:10.1021/ja4126609

Reference yield: 84.0%

methyl octanate (111-11-5) + cyclohexylamine (108-91-8,157973-60-9) → N-(cyclohexyl)-n-octanoylamide (42577-04-8)

Guidance literature:

With 1,2,4-Triazole; 1,8-diazabicyclo[5.4.0]undec-7-ene; at 95 ℃; for 24h;

DOI:10.1021/ol900098q

upstream raw materials:

cyclohexylamine

n-octanoic acid chloride

octanoic acid ethyl ester

Octanoic acid