4-nitro-N-pentylbenzenesulfonamide

Base Information

Chemical Name:4-nitro-N-pentylbenzenesulfonamide
CAS No.:52374-23-9
Molecular Formula:C₁₁H₁₆N₂O₄S
Molecular Weight:272.325
Hs Code.:
DSSTox Substance ID:DTXSID201297294

Synonyms:4-nitro-N-pentylbenzenesulfonamide;52374-23-9;DTXSID201297294;AKOS003836180

Suppliers and Price of 4-nitro-N-pentylbenzenesulfonamide

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 4-nitro-N-pentylbenzenesulfonamide

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:272.08307817
Heavy Atom Count:18
Complexity:350

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of 4-nitro-N-pentylbenzenesulfonamide

There total 2 articles about 4-nitro-N-pentylbenzenesulfonamide 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:

: 110-58-7
n-Pentylamine

: 98-74-8
4-Nitrobenzenesulfonyl chloride

: 52374-23-9
4-nitro-N-pentylbenzenesulfonamide

Guidance literature:: With sodium hydroxide; In N,N-dimethyl-formamide;
DOI:10.1021/jo00938a017

Reference yield:

: 52374-23-9
4-nitro-N-pentylbenzenesulfonamide

Guidance literature:: Pentylamin, p-Nitrobenzolsulfonylchlorid;

Reference yield: 63.0%

: 52374-23-9
4-nitro-N-pentylbenzenesulfonamide

: N-(4-bromopentyl)-4-nitrobenzenesulfonamide

: 122647-22-7
tetrabutylammonium hydrogen phthalate

Guidance literature:: With phthaloyl peroxide; tetrabutylammomium bromide; acetic acid; In 1,2-dichloro-ethane; at 20 ℃; for 12h; Reagent/catalyst; Inert atmosphere; Irradiation; Schlenk technique;
DOI:10.1021/acs.joc.8b00243