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(Trifluorosilyl)styrene, also known as 1-(trifluorosilyl)-1-phenylethene, is an organosilicon compound with the chemical formula C8H7F3Si. It is a colorless liquid that is sensitive to air and moisture, and it is typically stored under an inert atmosphere. (trifluorosilyl)styrene is characterized by the presence of a styrene moiety (a vinylbenzene group) attached to a trifluorosilyl group (SiF3). It is synthesized by reacting styrene with trifluorosilane in the presence of a catalyst, and it finds applications in the synthesis of various organosilicon compounds and as a precursor in the production of specialty materials. Due to its reactivity, it is used with caution in chemical processes and is an important intermediate in the field of organosilicon chemistry.

705-92-0

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705-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 705-92-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 705-92:
(5*7)+(4*0)+(3*5)+(2*9)+(1*2)=70
70 % 10 = 0
So 705-92-0 is a valid CAS Registry Number.

705-92-0Downstream Products

705-92-0Relevant academic research and scientific papers

Monodentate non-C2-symmetric chiral N-heterocyclic carbene complexes for enantioselective synthesis. Cu-catalyzed conjugate additions of aryl- and alkenylsilylfluorides to cyclic enones

Lee, Kang-Sang,Hoveyda, Amir H.

body text, p. 4455 - 4462 (2009/09/30)

(Chemical Equation Presented) A new class of enantioselective conjugate addition (ECA) reactions that involve aryl- or alkenylsilyl fluoride reagents and are catalyzed by chiral non-C2-symmetric Cu-based N-heterocyclic carbene (NHC) complexes a

Diastereoselective Addition of Carbon Electrophiles to Styrylsilanes: The Dimerization of β-(E)-(Halosilyl)styrenes

Brook, Michael A.,Sebastian, Thomas,Jueschke, Ralf,Dallaire, Carol

, p. 2273 - 2274 (2007/10/02)

β-(Halosilyl)styrenes undergo dimerization and trimerization reactions leading to 1,2,3-trisubstituted 1H-dihydroindenes with high diastereoselectivity.

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