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N-Benzyl-1,1,1-triphenoxysilanamine

Base Information
  • Chemical Name:N-Benzyl-1,1,1-triphenoxysilanamine
  • CAS No.:87498-96-2
  • Molecular Formula:C25H23NO3Si
  • Molecular Weight:413.548
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50524180
  • Wikidata:Q82390854
N-Benzyl-1,1,1-triphenoxysilanamine

Synonyms:N-Benzyl-1,1,1-triphenoxysilanamine;87498-96-2;DTXSID50524180

Suppliers and Price of N-Benzyl-1,1,1-triphenoxysilanamine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-Benzyl-1,1,1-triphenoxysilanamine
Chemical Property:
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:9
  • Exact Mass:413.14472013
  • Heavy Atom Count:30
  • Complexity:417
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CN[Si](OC2=CC=CC=C2)(OC3=CC=CC=C3)OC4=CC=CC=C4
Technology Process of N-Benzyl-1,1,1-triphenoxysilanamine

There total 1 articles about N-Benzyl-1,1,1-triphenoxysilanamine 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:
Guidance literature:
In not given; SnCl4 in CCl4, CH2Cl2 or petroleum ether was added dropwise into a soln. of ligand in the same solvent at -20 to -5°C and in the molar ratio (acid:base) 1:1.5; ppt. was filtered cold, washed, dried; elem.anal.;
DOI:10.1016/S0020-1693(00)81023-3
Guidance literature:
In not given; byproducts: tetraphenoxy silane; under N2, TiCl4 in CCl4, CH2Cl2 or petroleum ether added dropwise to soln. of ligand (molar ratio 1:1.5) in same solvent at -20 to -5°C; filtered cold, washed, dried; elem. anal.;
DOI:10.1016/S0020-1693(00)90849-1
upstream raw materials:

triphenoxychlorosilane

benzylamine

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