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N-hexyl-2-nitrobenzenesulfonamide

Base Information
  • Chemical Name:N-hexyl-2-nitrobenzenesulfonamide
  • CAS No.:89840-67-5
  • Molecular Formula:C12H18N2O4S
  • Molecular Weight:286.352
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20385487
  • Wikidata:Q82178304
  • ChEMBL ID:CHEMBL192376
N-hexyl-2-nitrobenzenesulfonamide

Synonyms:N-hexyl-2-nitrobenzenesulfonamide;89840-67-5;CHEMBL192376;Benzenesulfonamide, N-hexyl-2-nitro-;CBDivE_014618;DTXSID20385487;N-Hexyl-2-nitro-benzenesulfonamide;BDBM50164220;STK036352;AKOS002935813;SR-01000200584;SR-01000200584-1

Suppliers and Price of N-hexyl-2-nitrobenzenesulfonamide
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
  • American Custom Chemicals Corporation
  • N-HEXYL-2-NITROBENZENESULFONAMIDE 95.00%
  • 5MG
  • $ 496.52
Total 0 raw suppliers
Chemical Property of N-hexyl-2-nitrobenzenesulfonamide
Chemical Property:
  • PSA:100.37000 
  • LogP:4.44830 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:7
  • Exact Mass:286.09872823
  • Heavy Atom Count:19
  • Complexity:372
Purity/Quality:

N-HEXYL-2-NITROBENZENESULFONAMIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCNS(=O)(=O)C1=CC=CC=C1[N+](=O)[O-]
Technology Process of N-hexyl-2-nitrobenzenesulfonamide

There total 9 articles about N-hexyl-2-nitrobenzenesulfonamide 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:
Guidance literature:
With hydrogen; In methanol; at 25 ℃; for 10h; chemoselective reaction;
DOI:10.1021/ol4002448
Guidance literature:
Multi-step reaction with 3 steps
1: azodicarboxylic acid bis(2-methoxyethyl) ester; triphenylphosphine / toluene / 12 h / 20 °C / Inert atmosphere
2: trifluoroacetic acid / dichloromethane / 12 h / 20 °C / Inert atmosphere
3: hydrogen / methanol / 10 h / 25 °C
With azodicarboxylic acid bis(2-methoxyethyl) ester; hydrogen; triphenylphosphine; trifluoroacetic acid; In methanol; dichloromethane; toluene;
DOI:10.1021/ol4002448
Guidance literature:
Multi-step reaction with 2 steps
1: trifluoroacetic acid / dichloromethane / 12 h / 20 °C / Inert atmosphere
2: hydrogen / methanol / 10 h / 25 °C
With hydrogen; trifluoroacetic acid; In methanol; dichloromethane;
DOI:10.1021/ol4002448
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