Boroxin, trihexyl-

Base Information

• Chemical Name: Boroxin, trihexyl-
• CAS No.: 7325-10-2
• Molecular Formula: C18H39B3O3
• Molecular Weight: 335.939
• DSSTox Substance ID: DTXSID50461768
• Wikidata: Q82286180
• Mol file: 7325-10-2.mol

Synonyms:Boroxin, trihexyl-;7325-10-2;SCHEMBL7863075;DTXSID50461768

Chemical Property of Boroxin, trihexyl-

Chemical Property:

• Vapor Pressure: 2.39E-05mmHg at 25°C
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 15
• Exact Mass: 336.3178356
• Heavy Atom Count: 24
• Complexity: 227

Purity/Quality:

95% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: B1(OB(OB(O1)CCCCCC)CCCCCC)CCCCCC

Technology Process of Boroxin, trihexyl-

There total 1 articles about Boroxin, trihexyl- 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: 9.4%

2-Hexyl-1,3,2-dithiaborolane (88686-82-2) + dimethylsulfoxonium methylide (70775-39-2,5367-24-8) → 2-methylsulfanyl-ethanethiol (22322-43-6) + 1,2-bis(methylthio)ethane (6628-18-8) + n-hexylboroxine (7325-10-2) + hexan-1-ol (111-27-3)

Guidance literature:

With trimethylamine-N-oxide dihydrate; In toluene; treated with 1 equiv. of ylide (0-24°C, 30 min); oxidized with trimethylamine-N-oxide dihydrate (3 equiv.) (60°C, 2 h); GCMS;

DOI:10.1039/b311292f

upstream raw materials:

2-Hexyl-1,3,2-dithiaborolane

dimethylsulfoxonium methylide

Refernces