Benzenesulfonamide, N-(2-(4-((((butylamino)carbonyl)amino)sulfonyl)phenyl)ethyl)-2-methoxy-5-nitro-

Base Information

Chemical Name:Benzenesulfonamide, N-(2-(4-((((butylamino)carbonyl)amino)sulfonyl)phenyl)ethyl)-2-methoxy-5-nitro-
CAS No.:81514-29-6
Molecular Formula:C20H26N4O8S2
Molecular Weight:514.5724
Hs Code.:
DSSTox Substance ID:DTXSID30231163
Wikidata:Q83111998

Synonyms:BRN 5676942;Benzenesulfonamide, N-(2-(4-((((butylamino)carbonyl)amino)sulfonyl)phenyl)ethyl)-2-methoxy-5-nitro-;81514-29-6;DTXSID30231163;C20H26N4O8S2;LS-31339

Suppliers and Price of Benzenesulfonamide, N-(2-(4-((((butylamino)carbonyl)amino)sulfonyl)phenyl)ethyl)-2-methoxy-5-nitro-

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 Benzenesulfonamide, N-(2-(4-((((butylamino)carbonyl)amino)sulfonyl)phenyl)ethyl)-2-methoxy-5-nitro-

Chemical Property:

Density:1.369g/cm³
XLogP3:2.5
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:11
Exact Mass:514.11920615
Heavy Atom Count:34
Complexity:872

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCNC(=O)NS(=O)(=O)C1=CC=C(C=C1)CCNS(=O)(=O)C2=C(C=CC(=C2)[N+](=O)[O-])OC

Technology Process of Benzenesulfonamide, N-(2-(4-((((butylamino)carbonyl)amino)sulfonyl)phenyl)ethyl)-2-methoxy-5-nitro-

There total 3 articles about Benzenesulfonamide, N-(2-(4-((((butylamino)carbonyl)amino)sulfonyl)phenyl)ethyl)-2-methoxy-5-nitro- 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: 86.0%

: 81514-23-0
2-Methoxy-5-nitro-N-[2-(4-sulfamoyl-phenyl)-ethyl]-benzenesulfonamide

: 111-36-4
n-butyl isocyanide

: 81514-29-6
C₂₀H₂₆N₄O₈S₂

Guidance literature:: With sodium carbonate; In acetone; for 8h; Heating;

Reference yield:

: 81118-92-5
2-methoxy-5-nitrobenzene-1-sulfonyl chloride

: 81514-29-6
C₂₀H₂₆N₄O₈S₂

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / triethylamine / diethyl ether; ethanol / 0.75 h / Heating

2: 86 percent / Na₂CO₃ / acetone / 8 h / Heating

With sodium carbonate; triethylamine; In diethyl ether; ethanol; acetone;

Reference yield:

: 6325-22-0,42286-14-6
chlorhydrate de (β-aminoethyl)-4 benzenesulfonamide

: 81514-29-6
C₂₀H₂₆N₄O₈S₂

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / triethylamine / diethyl ether; ethanol / 0.75 h / Heating

2: 86 percent / Na₂CO₃ / acetone / 8 h / Heating

With sodium carbonate; triethylamine; In diethyl ether; ethanol; acetone;