4-amino-N-(4-butylphenyl)benzamide

Base Information

Chemical Name:4-amino-N-(4-butylphenyl)benzamide
CAS No.:89092-37-5
Molecular Formula:C17H20N2O
Molecular Weight:268.359
Hs Code.:
DSSTox Substance ID:DTXSID20536811
Wikidata:Q82411582

Synonyms:4-amino-N-(4-butylphenyl)benzamide;89092-37-5;SCHEMBL10803698;DTXSID20536811;AKOS009490358;AQ-390/43490519

Suppliers and Price of 4-amino-N-(4-butylphenyl)benzamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of 4-amino-N-(4-butylphenyl)benzamide

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:268.157563266
Heavy Atom Count:20
Complexity:289

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCC1=CC=C(C=C1)NC(=O)C2=CC=C(C=C2)N

Technology Process of 4-amino-N-(4-butylphenyl)benzamide

There total 4 articles about 4-amino-N-(4-butylphenyl)benzamide 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:

: 99338-13-3
4'-butyl-4-nitrobenzanilide

: 89092-37-5
4'-butyl-4-aminobenzanilide

Guidance literature:: With hydrogenchloride; tin; In tetrahydrofuran; at 50 ℃; for 1h;
DOI:10.1021/jm00153a018

Reference yield:

: 104-13-2
4-Butylaniline

: 89092-37-5
4'-butyl-4-aminobenzanilide

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 0.08 h / Ambient temperature

2: Sn, 6 N HCl / tetrahydrofuran / 1 h / 50 °C

With hydrogenchloride; tin; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00153a018

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 89092-37-5
4'-butyl-4-aminobenzanilide

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / CH₂Cl₂ / 0.08 h / Ambient temperature

2: Sn, 6 N HCl / tetrahydrofuran / 1 h / 50 °C

With hydrogenchloride; tin; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00153a018