Benzenesulfonamide, N-3-butenyl-4-methyl-N-4-pentenyl-

Base Information

Chemical Name:Benzenesulfonamide, N-3-butenyl-4-methyl-N-4-pentenyl-
CAS No.:436804-26-1
Molecular Formula:C16H23NO2S
Molecular Weight:293.43
Hs Code.:
DSSTox Substance ID:DTXSID70457047
Nikkaji Number:J1.712.461G
Wikidata:Q82279728

Synonyms:436804-26-1;Benzenesulfonamide, N-3-butenyl-4-methyl-N-4-pentenyl-;SCHEMBL13625327;DTXSID70457047;N-Tosyl(3-butenyl)(4-pentenyl)amine

Suppliers and Price of Benzenesulfonamide, N-3-butenyl-4-methyl-N-4-pentenyl-

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 Benzenesulfonamide, N-3-butenyl-4-methyl-N-4-pentenyl-

Chemical Property:

PSA：45.76000
LogP:4.60880
XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:9
Exact Mass:293.14495015
Heavy Atom Count:20
Complexity:389

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)N(CCCC=C)CCC=C

Technology Process of Benzenesulfonamide, N-3-butenyl-4-methyl-N-4-pentenyl-

There total 3 articles about Benzenesulfonamide, N-3-butenyl-4-methyl-N-4-pentenyl- 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:

: 627-27-0
homoalylic alcohol

: 81097-24-7
N-tosyl-(4-pentenyl)amine

: 436804-26-1
N-(but-3-en-1-yl)-4-methyl-N-(pent-4-en-1-yl)benzenesulfonamide

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; toluene; at 0 - 20 ℃; for 4h; Solvent;

Reference yield:

: 913361-16-7
N-(but-3-enyl)pent-4-en-1-amine

: 98-59-9
p-toluenesulfonyl chloride

: 436804-26-1
N-(but-3-en-1-yl)-4-methyl-N-(pent-4-en-1-yl)benzenesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃;
DOI:10.1002/chem.201202207

Reference yield:

: 70-55-3
toluene-4-sulfonamide

: 436804-26-1
N-(but-3-en-1-yl)-4-methyl-N-(pent-4-en-1-yl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 61 percent / K₂CO₃ / acetone

2: 86 percent / NaH / dimethylformamide

With sodium hydride; potassium carbonate; In N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.tetlet.2003.10.191