4-chloro-N-(4-hydroxy-1-naphthyl)benzenesulfonamide

Base Information

Chemical Name:4-chloro-N-(4-hydroxy-1-naphthyl)benzenesulfonamide
CAS No.:139719-06-5
Molecular Formula:C16H12ClNO3S
Molecular Weight:333.795
Hs Code.:
Mol file:139719-06-5.mol

Synonyms:4-p-Chlorophenylsulfonylamino-1-naphthol;N-p-chlorophenylsulfonyl-1,4-aminonaphthol;4-Chloro-N-(4-hydroxy-naphthalen-1-yl)-benzenesulfonamide;

Suppliers and Price of 4-chloro-N-(4-hydroxy-1-naphthyl)benzenesulfonamide

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 0 raw suppliers

Chemical Property of 4-chloro-N-(4-hydroxy-1-naphthyl)benzenesulfonamide

Chemical Property:

PSA：74.78000
LogP:5.15340

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-chloro-N-(4-hydroxy-1-naphthyl)benzenesulfonamide

There total 4 articles about 4-chloro-N-(4-hydroxy-1-naphthyl)benzenesulfonamide 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%

: 2834-90-4
4-amino-1-naphthol

: 98-60-2
4-chlorobenzenesulfonyl chloride

: 139719-06-5
4-chloro-N-(4-hydroxynaphthalen-1-yl)benzenesulfonamide

Guidance literature:: at 0 - 20 ℃; for 5h;
DOI:10.1016/j.bmc.2013.11.052

Reference yield: 81.0%

: 236739-38-1
4-chloro-N-(2,3-dibromo-4-oxo-3,4-dihydro-2H-naphthalen-1-ylidene)-benzenesulfonamide

: 139719-06-5
4-chloro-N-(4-hydroxynaphthalen-1-yl)benzenesulfonamide

Guidance literature:: With zinc; In acetic acid;

Reference yield:

: 86-57-7
1-Nitronaphthalene

: 139719-06-5
4-chloro-N-(4-hydroxynaphthalen-1-yl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: tert.-butylhydroperoxide; potassium hydroxide / dimethyl sulfoxide; water

2: palladium on activated charcoal; hydrogen / methanol

3: 5 h / 0 - 20 °C

With tert.-butylhydroperoxide; palladium on activated charcoal; hydrogen; potassium hydroxide; In methanol; water; dimethyl sulfoxide;
DOI:10.1016/j.bmc.2013.11.052