2-Ethyl-N-methylhexanamide

Base Information

• Chemical Name: 2-Ethyl-N-methylhexanamide
• CAS No.: 1114-75-6
• Molecular Formula: C9H19 N O
• Molecular Weight: 157.2533
• NSC Number: 38806
• ChEMBL ID: CHEMBL1081421
• Mol file: 1114-75-6.mol

Synonyms:2-Ethyl-N-methylhexanamide;NSC 38806;HEXANAMIDE, 2-ETHYL-N-METHYL-;BRN 1754559;1114-75-6;NSC38806;SCHEMBL2106254;CHEMBL1081421;NSC-38806;AKOS009163595;LS-74973

Chemical Property of 2-Ethyl-N-methylhexanamide

Chemical Property:

• Vapor Pressure: 0.0398mmHg at 25°C
• Boiling Point: 239.6°Cat760mmHg
• Flash Point: 135.1°C
• Density: 0.857g/cm³
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 157.146664230
• Heavy Atom Count: 11
• Complexity: 112

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCC(CC)C(=O)NC

Technology Process of 2-Ethyl-N-methylhexanamide

There total 5 articles about 2-Ethyl-N-methylhexanamide 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:

2-Ethylhexanoic acid (149-57-5) + methylamine (74-89-5) → α-Ethyl-capronsaeure-methylamid (1114-75-6)

Guidance literature:

In ethanol; at 120 - 190 ℃;

Reference yield:

2-ethylhexanoic acid chloride (760-67-8) → α-Ethyl-capronsaeure-methylamid (1114-75-6)

Guidance literature:

With methylamine; In dichloromethane; water; at 0 ℃; for 2h;

DOI:10.1021/jm901229s

Reference yield:

methylamine (74-89-5) → α-Ethyl-capronsaeure-methylamid (1114-75-6)

Guidance literature:

DOI:10.1021/ja01279a024

upstream raw materials:

ethyl-butyl-malonic acid diethyl ester

methylamine

diethyl butylmalonate

2-Ethylhexanoic acid

Downstream raw materials:

N-methyl-2-ethylhexanamine