Butanamide, N-propyl-

Base Information

• Chemical Name: Butanamide, N-propyl-
• CAS No.: 5129-73-7
• Molecular Formula: C7H15NO
• Molecular Weight: 129.202
• NSC Number: 26636
• UNII: DMV7258F72
• DSSTox Substance ID: DTXSID70282578
• Nikkaji Number: J581.332H
• Wikidata: Q82016889
• Mol file: 5129-73-7.mol

Synonyms:n-Propylbutanamide;Butanamide, N-propyl-;N-propyl-butyramide;5129-73-7;N-Propylbutyramide;Butyramide, N-propyl-;DMV7258F72;NSC-26636;NSC26636;n-Propylbutanamide #;N-n-propyl-butyramide;SCHEMBL840681;UNII-DMV7258F72;DTXSID70282578;STR01196;NSC 26636;AKOS003856254

Chemical Property of Butanamide, N-propyl-

Chemical Property:

• Vapor Pressure: 0.0854mmHg at 25°C
• Boiling Point: 225.7°Cat760mmHg
• Flash Point: 122.3°C
• Density: 0.861g/cm³
• XLogP3: 1.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 129.115364102
• Heavy Atom Count: 9
• Complexity: 81

Purity/Quality:

99%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCC(=O)NCCC

Technology Process of Butanamide, N-propyl-

There total 8 articles about Butanamide, N-propyl- 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: 70.0%

4-heptanone (123-19-3) → N-propylbutyrylamide (5129-73-7)

Guidance literature:

With hydrogen azide; titanium tetrachloride; In methanol; chloroform; for 48h; Ambient temperature;

DOI:10.1021/jo00236a006

Reference yield: 50.0%

propylamine (107-10-8,42939-71-9) + butyryl chloride (141-75-3) → N-propylbutyrylamide (5129-73-7)

Guidance literature:

With potassium carbonate; In water; ethyl acetate;

DOI:10.1021/ol0342195

Reference yield:

propylamine (107-10-8,42939-71-9) + N-butylamine (109-73-9,85404-21-3) + butyryl chloride (141-75-3) → N-propylbutyrylamide (5129-73-7) + N-butyl-butyramide (10264-16-1) + butyric acid (107-92-6)

Guidance literature:

N-butylamine; butyryl chloride; With sodium hydroxide; In water; at 25 ℃; Flow reactor;

propylamine; In water; at 25 ℃; Flow reactor;

upstream raw materials:

propylamine

butanoic acid anhydride

butyryl chloride

4-heptanone

Downstream raw materials:

N-propionylbutyramide

Refernces

• 1、 -. "PRODUCTION METHOD OF AMIDE COMPOUND". Paragraph 0130-0133. . Retrieved 2020/10/08.
• 2、 Zyryanov, Grigory V.,Rudkevich, Dmitry M.. "Encapsulated reagents for nitrosation". . p. 1253 - 1256. Retrieved 2007/10/03.