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tetrabutylammonium bis<α,α-bis(trifluoromethyl)benzenemethanolato(2-)-C2,O><3,5-bis(trifluoromethyl)phenyl>silicate (1-)

Base Information Edit
  • Chemical Name:tetrabutylammonium bis<α,α-bis(trifluoromethyl)benzenemethanolato(2-)-C2,O><3,5-bis(trifluoromethyl)phenyl>silicate (1-)
  • CAS No.:97878-08-5
  • Molecular Formula:C16H36N*C26H11F18O2Si
  • Molecular Weight:967.897
  • Hs Code.:
  • Mol file:97878-08-5.mol
tetrabutylammonium bis<α,α-bis(trifluoromethyl)benzenemethanolato(2-)-C<sup>2</sup>,O><3,5-bis(trifluoromethyl)phenyl>silicate (1-)

Synonyms:tetrabutylammonium bis<α,α-bis(trifluoromethyl)benzenemethanolato(2-)-C2,O><3,5-bis(trifluoromethyl)phenyl>silicate (1-)

Suppliers and Price of tetrabutylammonium bis<α,α-bis(trifluoromethyl)benzenemethanolato(2-)-C2,O><3,5-bis(trifluoromethyl)phenyl>silicate (1-)
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of tetrabutylammonium bis<α,α-bis(trifluoromethyl)benzenemethanolato(2-)-C2,O><3,5-bis(trifluoromethyl)phenyl>silicate (1-) Edit
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Technology Process of tetrabutylammonium bis<α,α-bis(trifluoromethyl)benzenemethanolato(2-)-C2,O><3,5-bis(trifluoromethyl)phenyl>silicate (1-)

There total 7 articles about tetrabutylammonium bis<α,α-bis(trifluoromethyl)benzenemethanolato(2-)-C2,O><3,5-bis(trifluoromethyl)phenyl>silicate (1-) 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:
Multi-step reaction with 2 steps
1: 75 percent / Br2 / 24 h / 25 °C
2: 73.8 percent / diethyl ether; CH2Cl2 / 1.) -78 deg C, 30 min.; 2.) 25 deg C, 1 h
With bromine; In diethyl ether; dichloromethane;
DOI:10.1021/ja00308a030
Guidance literature:
Multi-step reaction with 3 steps
1: 59.6 percent / CH2Cl2
2: 72 percent / Br2 / 24 h / 25 °C
3: 73.8 percent / diethyl ether; CH2Cl2 / 1.) -78 deg C, 30 min.; 2.) 25 deg C, 1 h
With bromine; In diethyl ether; dichloromethane;
DOI:10.1021/ja00308a030
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