N-butyl-4-hydroxybenzenesulfonamide

Base Information

Chemical Name:N-butyl-4-hydroxybenzenesulfonamide
CAS No.:3077-63-2
Molecular Formula:C₁₀H₁₅NO₃S
Molecular Weight:229.3
Hs Code.:
European Community (EC) Number:834-620-5
DSSTox Substance ID:DTXSID001294349
Mol file:3077-63-2.mol

Synonyms:3077-63-2;N-butyl-4-hydroxybenzene-1-sulfonamide;N-butyl-4-hydroxybenzenesulfonamide;Benzenesulfonamide, N-butyl-4-hydroxy-;SCHEMBL10908184;DTXSID001294349;AKOS009292087;FT-0730499;EN300-201154;Z381036314

Suppliers and Price of N-butyl-4-hydroxybenzenesulfonamide

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 N-butyl-4-hydroxybenzenesulfonamide

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:229.07726451
Heavy Atom Count:15
Complexity:263

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCNS(=O)(=O)C1=CC=C(C=C1)O

Technology Process of N-butyl-4-hydroxybenzenesulfonamide

There total 5 articles about N-butyl-4-hydroxybenzenesulfonamide 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: 10.0%

: 4025-67-6
4-hydroxybenzene-1-sulfonyl chloride

: 109-73-9,85404-21-3
N-butylamine

: 4-hydroxy-benzenesulfonic acid 4-butylsulfamoyl-phenyl ester

: C₂₂H₂₃NO₉S₃

: 3077-63-2
N-butyl-4-hydroxybenzenesulfonamide

Guidance literature:: With triethylamine; In chloroform; at 20 ℃; for 10h;
DOI:10.1081/SCC-200026214

Reference yield:

: N-butyl-4-trimethylsilanyloxy-benzenesulfonamide

: 3077-63-2
N-butyl-4-hydroxybenzenesulfonamide

Guidance literature:: With methanol; In chloroform; at 65 ℃; for 1h;
DOI:10.1081/SCC-200026214

Reference yield:

: 4-(trimethylsilyloxy)benzenesulfonyl chloride

: 3077-63-2
N-butyl-4-hydroxybenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / CHCl₃ / 10 h / 20 °C

2: methanol / CHCl₃ / 1 h / 65 °C

With methanol; triethylamine; In chloroform;
DOI:10.1081/SCC-200026214