N1-(4-propylphenyl)acetamide

Base Information

• Chemical Name: N1-(4-propylphenyl)acetamide
• CAS No.: 20330-99-8
• Molecular Formula: C11H15 N O
• Molecular Weight: 177.246
• Hs Code.: 2924299090
• DSSTox Substance ID: DTXSID90876498
• Nikkaji Number: J1.605.837H
• Wikidata: Q82858144
• Mol file: 20330-99-8.mol

Synonyms:N1-(4-propylphenyl)acetamide;20330-99-8;N-(4-propylphenyl)acetamide;acetamide, N-(4-propylphenyl)-;4-n-Propylacetanilide;4-propylacetanilide;Maybridge1_001001;SCHEMBL7211903;HMS544F11;DTXSID90876498;MFCD00275765;AKOS006227941;TS-02466;CS-0362323;FT-0629682;W-206503

Chemical Property of N1-(4-propylphenyl)acetamide

Chemical Property:

• Vapor Pressure: 0.000111mmHg at 25°C
• Melting Point: 98-100
• Refractive Index: 1.549
• Boiling Point: 336.6°Cat760mmHg
• Flash Point: 199.2°C
• PSA: 29.10000
• Density: 1.031g/cm³
• LogP: 2.67050
• XLogP3: 2.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 177.115364102
• Heavy Atom Count: 13
• Complexity: 160

Purity/Quality:

98%min ^*data from raw suppliers

N1-(4-Propylphenyl)acetamide 97% ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: R22:Harmful if swallowed.

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCC1=CC=C(C=C1)NC(=O)C

Technology Process of N1-(4-propylphenyl)acetamide

There total 5 articles about N1-(4-propylphenyl)acetamide 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:

N-(4-propionylphenyl)acetamide (16960-49-9) → 4-propylacetanilide (20330-99-8)

Guidance literature:

With Pd-BaSO₄; perchloric acid; acetic acid; at 95 ℃; Hydrogenation;

DOI:10.1039/jr9530002066

Reference yield:

1-(4-aminophenyl)-1-propanone (70-69-9) → 4-propylacetanilide (20330-99-8)

Guidance literature:

With Pd-BaSO₄; perchloric acid; acetic acid; at 95 ℃; Hydrogenation;

DOI:10.1039/jr9530002066

Reference yield:

aniline (62-53-3) → 4-propylacetanilide (20330-99-8)

Guidance literature:

Multi-step reaction with 2 steps

1: ZnCl₂

With zinc(II) chloride;

upstream raw materials:

N-(4-propionylphenyl)acetamide

1-(4-aminophenyl)-1-propanone

1-(4-propylphenyl)ethan-1-one

4-propylaniline

Downstream raw materials:

2-Bromo-4-propyl-phenylamine

N-(2-Bromo-4-propyl-phenyl)-acetamide

phenyl-(4-propyl-phenyl)-amine

acetic acid-(2-nitro-4-propyl-anilide)