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CID 53425746

Base Information Edit
  • Chemical Name:CID 53425746
  • CAS No.:24628-33-9
  • Molecular Formula:F5H Si2
  • Molecular Weight:152.171
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10179372
  • Mol file:24628-33-9.mol
CID 53425746

Synonyms:DTXSID10179372

Suppliers and Price of CID 53425746
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
Total 0 raw suppliers
Chemical Property of CID 53425746 Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:0.00000 
  • Density:g/cm3 
  • LogP:1.07170 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:0
  • Exact Mass:150.94586888
  • Heavy Atom Count:7
  • Complexity:51.6
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:F[Si](F)[Si](F)(F)F
Technology Process of CID 53425746

There total 5 articles about CID 53425746 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 neat (no solvent); React. (vac. line, no solvent) at room temp. for 10 min.; Removal of Me3SnCl by passing the mixt. through a trap cooled to -95°C (toluene). IR and NMR spectra indicate presence of resulting compounds in approximately equimolar amt.;
Guidance literature:
In neat (no solvent); React. of equimolar amt. of starting materials (vac. line, room temp., 10 min).; Removal of Me3SnCl by passing the mixt. through a trap cooled to -95°C (toluene). IR identificatio of resulting compounds.;
Guidance literature:
In neat (no solvent); Warming mixt. of equimolar amt. of starting materials (condensed at -196°C) to -80°C (30 min) and then gradually to 10°C.; Removal of Me3SnCl by passing the mixt. through a trap cooled to -95°C (toluene). NMR spectrum indicate presence of major resulting compounds, with small amt. of SiF3SiHBr2 and unreacted SiF3SiFHBr.;
Refernces Edit
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