N-heptyl-4-nitrobenzenesulfonamide

Base Information

Chemical Name:N-heptyl-4-nitrobenzenesulfonamide
CAS No.:107618-53-1
Molecular Formula:C₁₃H₂₀N₂O₄S
Molecular Weight:300.379
Hs Code.:
DSSTox Substance ID:DTXSID401297414

Synonyms:N-heptyl-4-nitrobenzenesulfonamide;DTXSID401297414;AKOS003835265;107618-53-1

Suppliers and Price of N-heptyl-4-nitrobenzenesulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-heptyl-4-nitrobenzenesulfonamide

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:300.11437830
Heavy Atom Count:20
Complexity:378

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCNS(=O)(=O)C1=CC=C(C=C1)[N+](=O)[O-]

Technology Process of N-heptyl-4-nitrobenzenesulfonamide

There total 2 articles about N-heptyl-4-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:

Reference yield: 25.0%

: 111-68-2
1-Heptylamine

: 98-74-8
4-Nitrobenzenesulfonyl chloride

: 107618-53-1
N-heptyl-4-nitrobenzenesulfonamide

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; for 12h;
DOI:10.1002/anie.201604704

Reference yield:

: 107618-53-1
N-heptyl-4-nitrobenzenesulfonamide

Guidance literature:: Heptylamin, p-Nitrobenzolsulfonylchlorid;

Reference yield: 90.0%

: 107618-53-1
N-heptyl-4-nitrobenzenesulfonamide

: N-chloro-N-heptyl-4-nitrobenzenesulfonamide

Guidance literature:: With phthaloyl peroxide; tetrabutyl-ammonium chloride; In 1,2-dichloro-ethane; at 20 ℃; for 12h; Irradiation; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.joc.8b00243