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3,5-Bis[[(tert-Butyl)diMethylsilyl]oxy]benzeneMethanol

Base Information Edit
  • Chemical Name:3,5-Bis[[(tert-Butyl)diMethylsilyl]oxy]benzeneMethanol
  • CAS No.:103929-84-6
  • Molecular Formula:C19H36O3Si2
  • Molecular Weight:368.664
  • Hs Code.:
  • Mol file:103929-84-6.mol
3,5-Bis[[(tert-Butyl)diMethylsilyl]oxy]benzeneMethanol

Synonyms:3,5-Bis[[(tert-Butyl)dimethylsilyl]oxy]benzenemethanol;

Suppliers and Price of 3,5-Bis[[(tert-Butyl)diMethylsilyl]oxy]benzeneMethanol
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 3,5-Bis[[(tert-Butyl)dimethylsilyl]oxy]benzenemethanol
  • 2.5g
  • $ 1540.00
  • Medical Isotopes, Inc.
  • 3,5-Bis[[(tert-Butyl)dimethylsilyl]oxy]benzenemethanol
  • 2.5 g
  • $ 2400.00
  • American Custom Chemicals Corporation
  • 3,5-BIS[[(TERT-BUTYL)DIMETHYLSILYL]OXY]BENZENEMETHANOL 95.00%
  • 5MG
  • $ 505.33
Total 2 raw suppliers
Chemical Property of 3,5-Bis[[(tert-Butyl)diMethylsilyl]oxy]benzeneMethanol Edit
Chemical Property:
  • PSA:38.69000 
  • LogP:5.94690 
  • Solubility.:Ethyl Acetate, Hexanes 
Purity/Quality:

98%min *data from raw suppliers

3,5-Bis[[(tert-Butyl)dimethylsilyl]oxy]benzenemethanol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 3,5-Bis[[(tert-Butyl)dimethylsilyl]oxy]benzenemethanol is a reactant used in the synthesis of natural polyhydroxystilbenes.
Technology Process of 3,5-Bis[[(tert-Butyl)diMethylsilyl]oxy]benzeneMethanol

There total 10 articles about 3,5-Bis[[(tert-Butyl)diMethylsilyl]oxy]benzeneMethanol 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:
With lithium aluminium tetrahydride; In diethyl ether; for 2h; Ambient temperature;
DOI:10.1055/s-1998-2193
Guidance literature:
Guidance literature:
With sodium tetrahydroborate; In methanol; at 20 ℃; for 0.5h;
DOI:10.1021/acs.jnatprod.6b00861
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