2-amino-N-propylacetamide

Base Information

• Chemical Name: 2-amino-N-propylacetamide
• CAS No.: 62029-81-6
• Molecular Formula: C₅H₁₂N₂O
• Molecular Weight: 116.163
• European Community (EC) Number: 837-791-4
• DSSTox Substance ID: DTXSID40406981

Synonyms:2-amino-N-propylacetamide;62029-81-6;HMS1780P18;SCHEMBL1376469;DTXSID40406981;MFCD06655365;AKOS000206328;BS-29022;CS-0454285;EN300-12590;A868576

Chemical Property of 2-amino-N-propylacetamide

Chemical Property:

• Vapor Pressure: 0.00695mmHg at 25°C
• Boiling Point: 270.2°Cat760mmHg
• Flash Point: 117.2°C
• PSA: 58.61000
• Density: 0.962g/cm³
• LogP: 1.01190
• XLogP3: -0.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 116.094963011
• Heavy Atom Count: 8
• Complexity: 72.8

Purity/Quality:

97% ^*data from raw suppliers

2-Amino-N-propylacetamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCNC(=O)CN

Technology Process of 2-amino-N-propylacetamide

There total 1 articles about 2-amino-N-propylacetamide 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: 71.0%

propylamine (107-10-8,42939-71-9) + glycine (56-40-6,18875-39-3,25718-94-9) → 2-amino-N-propyl-acetamide (62029-81-6)

Guidance literature:

With tris(2,2,2-trifluoroethyl) borate; at 80 ℃; for 15h; under 760.051 Torr;

DOI:10.1039/c6cc05147b

Reference yield: 77.0%

phenylacetic acid (103-82-2) + 2-amino-N-propyl-acetamide (62029-81-6) → N-(2-oxo-2-(propylamino)ethyl)-2-phenylacetamide (25443-72-5)

Guidance literature:

With tris(2,2,2-trifluoroethyl) borate; at 125 ℃; for 6h; chemoselective reaction; Green chemistry;

DOI:10.1002/chem.201800372

Reference yield:

2-amino-N-propyl-acetamide (62029-81-6) + 5-Bromo-2-aminobenzoic acid (5794-88-7) → C12H16BrN3O2

Guidance literature:

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In DMP; at 20 ℃;

DOI:10.1016/j.bmcl.2011.04.022

upstream raw materials:

propylamine

glycine

Downstream raw materials:

C₂₉H₃₀N₄O₂

N-(2-oxo-2-(propylamino)ethyl)-2-phenylacetamide

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