Benzenesulfonamide, N-(2,2-dimethyl-4-pentenyl)-4-methyl-

Base Information

Chemical Name:Benzenesulfonamide, N-(2,2-dimethyl-4-pentenyl)-4-methyl-
CAS No.:95106-72-2
Molecular Formula:C14H21NO2S
Molecular Weight:267.392
Hs Code.:
DSSTox Substance ID:DTXSID30466251
Nikkaji Number:J1.831.434G
Wikidata:Q82292778

Synonyms:95106-72-2;Benzenesulfonamide, N-(2,2-dimethyl-4-pentenyl)-4-methyl-;DTXSID30466251;N-(2,2-dimethylpent-4-en-1-yl)-4-methylbenzene sulfonamide

Suppliers and Price of Benzenesulfonamide, N-(2,2-dimethyl-4-pentenyl)-4-methyl-

Supply Marketing:

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

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Chemical Property of Benzenesulfonamide, N-(2,2-dimethyl-4-pentenyl)-4-methyl-

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:267.12930009
Heavy Atom Count:18
Complexity:360

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)NCC(C)(C)CC=C

Technology Process of Benzenesulfonamide, N-(2,2-dimethyl-4-pentenyl)-4-methyl-

There total 8 articles about Benzenesulfonamide, N-(2,2-dimethyl-4-pentenyl)-4-methyl- 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: 97.0%

: 73604-46-3
2,2-dimethyl-1-amino-pent-4-ene

: 98-59-9
p-toluenesulfonyl chloride

: 95106-72-2
N-tosyl-(2,2-dimethyl)-pent-4-enylamine

Guidance literature:: 2,2-dimethyl-1-amino-pent-4-ene; p-toluenesulfonyl chloride; In dichloromethane; at 0 ℃; for 0.0833333h; Inert atmosphere; Glovebox;

With pyridine; In dichloromethane; at 0 - 20 ℃; for 12h; Inert atmosphere; Glovebox;
DOI:10.1021/acs.joc.0c02637