4-Amino-n-octylbenzenesulfonamide

Base Information

Chemical Name:4-Amino-n-octylbenzenesulfonamide
CAS No.:67491-89-8
Molecular Formula:C14H24N2O2S
Molecular Weight:284.423
Hs Code.:
NSC Number:74591
DSSTox Substance ID:DTXSID20986872
Nikkaji Number:J2.350.531B
Wikidata:Q82974952

Synonyms:67491-89-8;4-amino-n-octylbenzenesulfonamide;NSC74591;DTXSID20986872;NSC-74591;4-Amino-N-octylbenzene-1-sulfonamide;AKOS017560422

Suppliers and Price of 4-Amino-n-octylbenzenesulfonamide

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 5 raw suppliers

Chemical Property of 4-Amino-n-octylbenzenesulfonamide

Chemical Property:

Vapor Pressure:8.57E-08mmHg at 25°C
Boiling Point:435.7°C at 760 mmHg
Flash Point:217.3°C
Density:1.103g/cm³
XLogP3:3.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:9
Exact Mass:284.15584919
Heavy Atom Count:19
Complexity:317

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCNS(=O)(=O)C1=CC=C(C=C1)N

Technology Process of 4-Amino-n-octylbenzenesulfonamide

There total 5 articles about 4-Amino-n-octylbenzenesulfonamide 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: 98.0%

: 52374-21-7
N-n-octyl-4-nitrobenzenesulfonamide

N-n-octyl-4-aminobenzenesulfonamide: 67491-89-8
N-n-octyl-4-aminobenzenesulfonamide

Guidance literature:: With hydrogenchloride; tin(ll) chloride; In ethanol; for 5h; Heating;
DOI:10.1021/ja061606b

Reference yield: 84.0%

: 111-87-5
octanol

: 63-74-1
sulfanilamide

N-n-octyl-4-aminobenzenesulfonamide: 67491-89-8
N-n-octyl-4-aminobenzenesulfonamide

Guidance literature:: With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; caesium carbonate; In tert-Amyl alcohol; at 120 ℃; for 12h; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.orglett.5b00824

Reference yield:

: 111-86-4
n-Octylamine

N-n-octyl-4-aminobenzenesulfonamide: 67491-89-8
N-n-octyl-4-aminobenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / triethylamine / CH₂Cl₂ / 0.33 h / 20 °C

2: 98 percent / SnCl₂*2H₂O; aq. HCl / ethanol / 5 h / Heating

With hydrogenchloride; triethylamine; tin(ll) chloride; In ethanol; dichloromethane;
DOI:10.1021/ja061606b