N-(2-CHLOROPHENYL)-1-NAPHTHAMIDE

Base Information

Chemical Name:N-(2-CHLOROPHENYL)-1-NAPHTHAMIDE
CAS No.:77791-09-4
Molecular Formula:C17H12ClNO
Molecular Weight:281.741
Hs Code.:2924299090
Mol file:77791-09-4.mol

Synonyms:[1]Naphthoesaeure-(2-chlor-anilid);[1]naphthoic acid-(2-chloro-anilide);N-(2-CHLOROPHENYL)-1-NAPHTHAMIDE;

Suppliers and Price of N-(2-CHLOROPHENYL)-1-NAPHTHAMIDE

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

American Custom Chemicals Corporation
N-(2-CHLOROPHENYL)-1-NAPHTHAMIDE 95.00%
5MG
$ 499.64

Total 3 raw suppliers

Chemical Property of N-(2-CHLOROPHENYL)-1-NAPHTHAMIDE

Chemical Property:

PSA：29.10000
LogP:4.81850

Purity/Quality:

99% ^*data from raw suppliers

N-(2-CHLOROPHENYL)-1-NAPHTHAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of N-(2-CHLOROPHENYL)-1-NAPHTHAMIDE

There total 3 articles about N-(2-CHLOROPHENYL)-1-NAPHTHAMIDE 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: 83.0%

: 95-51-2
o-chloroaniline

: 879-18-5
naphthalene-1-carbonic acid chloride

: 77791-09-4
N-(2-chlorophenyl)naphthalene-1-carboxamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 12h;
DOI:10.3390/molecules190710386

Reference yield:

: 86-55-5
1-naphthalenecarboxylic acid

: 77791-09-4
N-(2-chlorophenyl)naphthalene-1-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / toluene / 2 h / Reflux

2: triethylamine / dichloromethane / 12 h / 20 °C

With thionyl chloride; triethylamine; In dichloromethane; toluene;
DOI:10.3390/molecules190710386