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Silane, trimethyl-7-oxabicyclo[4.1.0]hept-1-yl-

Base Information
  • Chemical Name:Silane, trimethyl-7-oxabicyclo[4.1.0]hept-1-yl-
  • CAS No.:60484-85-7
  • Molecular Formula:C9H18OSi
  • Molecular Weight:170.327
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70473464
  • Nikkaji Number:J914.935J
Silane, trimethyl-7-oxabicyclo[4.1.0]hept-1-yl-

Synonyms:Silane, trimethyl-7-oxabicyclo[4.1.0]hept-1-yl-;60484-85-7;DTXSID70473464;AKOS024330430;trimethyl(7-oxabicyclo[4.1.0]hept-1-yl)silane

Suppliers and Price of Silane, trimethyl-7-oxabicyclo[4.1.0]hept-1-yl-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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Total 1 raw suppliers
Chemical Property of Silane, trimethyl-7-oxabicyclo[4.1.0]hept-1-yl-
Chemical Property:
  • Boiling Point:90-93 °C(Press: 30 Torr) 
  • PSA:12.53000 
  • Density:0.93±0.1 g/cm3(Predicted) 
  • LogP:2.99530 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:170.112691728
  • Heavy Atom Count:11
  • Complexity:173
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C[Si](C)(C)C12CCCCC1O2
Technology Process of Silane, trimethyl-7-oxabicyclo[4.1.0]hept-1-yl-

There total 2 articles about Silane, trimethyl-7-oxabicyclo[4.1.0]hept-1-yl- 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 ruthenium(II) bisoxazoline; sodium hydrogencarbonate; isobutyraldehyde; In dichloromethane; at 20 ℃; for 11h;
DOI:10.1016/S0040-4020(03)01210-9
Guidance literature:
With 3,3-dimethyldioxirane; In acetone; Yield given. Yields of byproduct given; Ambient temperature;
DOI:10.1016/00404-0399(50)0960K-
Guidance literature:
With hydrogenchloride; In benzene; Product distribution; regioselectivity of the ring-opening of the title compound and 1-trimethylsilylcyclohexene with variuos nucleophiles; different solvents;
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