4-(3-Aminopropyl)benzene-1-sulfonamide

Base Information

Chemical Name:4-(3-Aminopropyl)benzene-1-sulfonamide
CAS No.:10079-78-4
Molecular Formula:C9H14N2O2S
Molecular Weight:214.288
Hs Code.:
DSSTox Substance ID:DTXSID40560698
Wikidata:Q82444279
Mol file:10079-78-4.mol

Synonyms:4-(3-aminopropyl)benzenesulfonamide;10079-78-4;4-(3-Aminopropyl)benzene-1-sulfonamide;SCHEMBL9683336;DTXSID40560698;QJFUYJHXJQEQCM-UHFFFAOYSA-N;4-(3-aminopropyl)benzenesulphonamide;AKOS015140728;3-(4-aminosulphonylphenyl)-propylamine;SB78917;EN300-376573

Suppliers and Price of 4-(3-Aminopropyl)benzene-1-sulfonamide

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
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price

Total 1 raw suppliers

Chemical Property of 4-(3-Aminopropyl)benzene-1-sulfonamide

Chemical Property:

XLogP3:-0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:214.07759887
Heavy Atom Count:14
Complexity:251

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1CCCN)S(=O)(=O)N

Technology Process of 4-(3-Aminopropyl)benzene-1-sulfonamide

There total 7 articles about 4-(3-Aminopropyl)benzene-1-sulfonamide 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: 80.0%

: 2,2,2-trifluoro-N-(3-(4-sulfamoylphenyl)propyl)acetamide

: 10079-78-4
p-β-(amino-n-propyl)-benzenesulfonamide

Guidance literature:: With water; potassium carbonate; In methanol; at 20 ℃; for 10h;
DOI:10.1016/j.ejmech.2016.04.015

Reference yield:

: 3240-35-5
4-formyl-benzenesulfonamide

: 2537-48-6
diethyl 1-cyanomethylphosphonate

: 10079-78-4
p-β-(amino-n-propyl)-benzenesulfonamide

: 88961-77-7
4-(2-cyano-ethyl)-benzenesulfonic acid amide

Guidance literature:: In tetrahydrofuran;

Reference yield:

: 77970-72-0
2,2,2-trifluoro-N-(3-phenyl-propyl)acetamide

: 10079-78-4
p-β-(amino-n-propyl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: chlorosulfonic acid / dichloromethane / 3 h / 0 - 20 °C

2: ammonia / dichloromethane / 0.5 h

3: water; potassium carbonate / methanol / 10 h / 20 °C

With chlorosulfonic acid; ammonia; water; potassium carbonate; In methanol; dichloromethane;
DOI:10.1016/j.ejmech.2016.04.015