Benzenesulfonamide, N-(di-2-furanylmethyl)-4-methyl-

Base Information

Chemical Name:Benzenesulfonamide, N-(di-2-furanylmethyl)-4-methyl-
CAS No.:488720-06-5
Molecular Formula:C16H15NO4S
Molecular Weight:317.365
Hs Code.:
DSSTox Substance ID:DTXSID10456357
Nikkaji Number:J1.784.021E
Wikidata:Q82278773

Synonyms:488720-06-5;N-(Di(furan-2-yl)methyl)-4-methylbenzenesulfonamide;Benzenesulfonamide, N-(di-2-furanylmethyl)-4-methyl-;DTXSID10456357;N-[Di(2-furyl)methyl]-p-toluenesulfonamide

Suppliers and Price of Benzenesulfonamide, N-(di-2-furanylmethyl)-4-methyl-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Benzenesulfonamide, N-(di-2-furanylmethyl)-4-methyl-

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:317.07217913
Heavy Atom Count:22
Complexity:437

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)NC(C2=CC=CO2)C3=CC=CO3

Technology Process of Benzenesulfonamide, N-(di-2-furanylmethyl)-4-methyl-

There total 5 articles about Benzenesulfonamide, N-(di-2-furanylmethyl)-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: 91.0%

: 110-00-9
furan

: 13707-47-6
2-furaldehyde tosylimine

: 488720-06-5
N-(1,1-difuran-2-ylmethyl)-4-methylbenzenesulfonamide

Guidance literature:: furan; With n-butyllithium; In tetrahydrofuran; hexane; at -5 ℃; for 1h;

2-furaldehyde tosylimine; In tetrahydrofuran; hexane; at -78 ℃; for 1h;
DOI:10.1039/b204904j

Reference yield: 91.0%

: 110-00-9
furan

: 109-72-8,29786-93-4
n-butyllithium

: 13707-47-6
2-furaldehyde tosylimine

: 488720-06-5
N-(1,1-difuran-2-ylmethyl)-4-methylbenzenesulfonamide

Guidance literature:: furan; n-butyllithium;

2-furaldehyde tosylimine; In tetrahydrofuran; at -78 ℃; Further stages.;
DOI:10.1055/s-2007-973875

Reference yield:

: 70-55-3
toluene-4-sulfonamide

: 488720-06-5
N-(1,1-difuran-2-ylmethyl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 95 percent / Ti(OEt)4 / CH₂Cl₂ / 50 °C

2.2: 91 percent / tetrahydrofuran / -78 °C

With titanium(IV) tetraethanolate; In dichloromethane;
DOI:10.1055/s-2007-973875