4-(dibutylamino)-3,5-dinitro-N-phenylbenzenesulfonamide

Base Information

Chemical Name:4-(dibutylamino)-3,5-dinitro-N-phenylbenzenesulfonamide
CAS No.:619267-15-1
Molecular Formula:C20H26N4O6S
Molecular Weight:450.516
Hs Code.:
DSSTox Substance ID:DTXSID10435526
Nikkaji Number:J2.362.470B
Wikidata:Q82250539
ChEMBL ID:CHEMBL55225

Synonyms:GB-II-150;N1-phenyl-3,5-dinitro-N4,N4-di-n-butylsulfanilamide

Suppliers and Price of 4-(dibutylamino)-3,5-dinitro-N-phenylbenzenesulfonamide

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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Total 0 raw suppliers

Chemical Property of 4-(dibutylamino)-3,5-dinitro-N-phenylbenzenesulfonamide

Chemical Property:

XLogP3:4.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:10
Exact Mass:450.15730574
Heavy Atom Count:31
Complexity:649

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCN(CCCC)C1=C(C=C(C=C1[N+](=O)[O-])S(=O)(=O)NC2=CC=CC=C2)[N+](=O)[O-]

Technology Process of 4-(dibutylamino)-3,5-dinitro-N-phenylbenzenesulfonamide

There total 4 articles about 4-(dibutylamino)-3,5-dinitro-N-phenylbenzenesulfonamide 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:

: 38185-06-7
potassium 4-chloro-3,5-dinitrobenzene sulfonate

: 619267-15-1
N₁-phenyl-3,5-dinitro-N₄,N₄-di-n-butylsulfanilamide

Guidance literature:: Multi-step reaction with 3 steps

1: 76 percent / methanol / 3 h / Heating

2: PCl₅ / CH₂Cl₂ / 2 h

3: 286 mg / pyridine / 3 h / 45 °C

With pyridine; phosphorus pentachloride; In methanol; dichloromethane;
DOI:10.1021/jm0304461

Reference yield:

: 111-92-2
dibutylamine

: 619267-15-1
N₁-phenyl-3,5-dinitro-N₄,N₄-di-n-butylsulfanilamide

Guidance literature:: Multi-step reaction with 3 steps

1: 76 percent / methanol / 3 h / Heating

2: PCl₅ / CH₂Cl₂ / 2 h

3: 286 mg / pyridine / 3 h / 45 °C

With pyridine; phosphorus pentachloride; In methanol; dichloromethane;
DOI:10.1021/jm0304461

Reference yield:

: potassium 3,5-dinitro-N⁴,N⁴-di-n-butylsulfonate

: 619267-15-1
N₁-phenyl-3,5-dinitro-N₄,N₄-di-n-butylsulfanilamide

Guidance literature:: Multi-step reaction with 2 steps

1: PCl₅ / CH₂Cl₂ / 2 h

2: 286 mg / pyridine / 3 h / 45 °C

With pyridine; phosphorus pentachloride; In dichloromethane;
DOI:10.1021/jm0304461