1-Hydroxy-N-phenyl-2-naphthalenecarboxamide

Base Information

Chemical Name:1-Hydroxy-N-phenyl-2-naphthalenecarboxamide
CAS No.:13545-65-8
Molecular Formula:C17H13NO2
Molecular Weight:263.296
Hs Code.:2924299090
Mol file:13545-65-8.mol

Synonyms:1-hydroxynaphthalene-2-carboxanilide;1-Hydroxy-2-naphthanilide;naphthol carboxylic acid anilide;2-Naphthalenecarboxamide, 1-hydroxy-N-phenyl-;1-hydroxy-[2]naphthoic acid anilide;1-hydroxy-N-phenyl-2-naphthalenecarboxamide;1-Hydroxy-[2]naphthoesaeure-anilid;1-hydroxy-naphthalene-2-carboxylic acid anilide;

Suppliers and Price of 1-Hydroxy-N-phenyl-2-naphthalenecarboxamide

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 4 raw suppliers

Chemical Property of 1-Hydroxy-N-phenyl-2-naphthalenecarboxamide

Chemical Property:

Vapor Pressure:1.07E-06mmHg at 25°C
Boiling Point:391.8oC at 760 mmHg
Flash Point:190.7oC
PSA：52.82000
Density:1.31g/cm3
LogP:4.18170

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 1-Hydroxy-N-phenyl-2-naphthalenecarboxamide

There total 17 articles about 1-Hydroxy-N-phenyl-2-naphthalenecarboxamide 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: 78.0%

: 62-53-3
aniline

: 86-48-6
1-hydroxy-2-naphthoic acid

: 13545-65-8
1-hydroxynaphthalene-2-carboxanilide

Guidance literature:: With phosphorus trichloride; In chlorobenzene; at 130 ℃; for 0.25h; Microwave irradiation;
DOI:10.1016/j.bmc.2013.08.030

Reference yield:

: 90-15-3
α-naphthol

: 13545-65-8
1-hydroxynaphthalene-2-carboxanilide

Guidance literature:: Multi-step reaction with 2 steps

1: aluminium chloride

2: lead (II)-oxide; ethanol

With aluminium trichloride; ethanol; lead(II) oxide;
DOI:10.1002/hlca.19320150133