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Trichloro-(2,2,2-trifluoro-1-fluoromethyl-ethyl)-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58293-48-4

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58293-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58293-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,9 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58293-48:
(7*5)+(6*8)+(5*2)+(4*9)+(3*3)+(2*4)+(1*8)=154
154 % 10 = 4
So 58293-48-4 is a valid CAS Registry Number.

58293-48-4Downstream Products

58293-48-4Relevant academic research and scientific papers

Catalytic Hydrosilylation of Hydrofluoroolefins (HFOs): Synthesis of New Fluorinated Silanes and Diversity of their Synthetic Character

Pavlenko, Natalia V.,Peng, Sheng,Petrov, Viacheslav,Jackson, Andrew,Sun, Xuehui,Sprague, Lee,Yagupolskii, Yurii L.

, p. 5425 - 5435 (2020)

New polyfluorinated silanes were synthesized via the Pt, Rh and Pd catalyzed hydrosilylation of commercially available hydrofluoroolefins (HFOs) in moderate to excellent yields. HFO-1234yf (2,3,3,3-tetrafluoropropene-1) and –1234ze (1,3,3,3-tetrafluoropropene-1) were reactive with Pt catalyst to form tetrafluoropropylsilanes along with defluorosilylation products. The Z- and E-isomers of HFO-1336mzz (1,1,1,4,4,4-hexafluorobut-2-ene) gave the desired silanes with Pd catalysis in good to excellent yields, while with Pt catalyst only the dehydrofluorination product CF2=CHCH2CF3 (HFO-1345czf, 1,1,4,4,4-pentafluorobut-1-ene) was obtained. Synthetic applications of the new polyfluorinated silanes were illustrated by conversion of dichloro(hexafluorobutyl)(methyl)silane to the cyclic trisiloxane, which can serve as a monomer for the preparation of polysiloxanes. In addition, the hexafluorobutylsilanes showed defluorinative reactivity with lithium reagents, thereby demonstrating their synthetic utility as valuable building blocks for further transformations via C–F and C-Si bond activation.

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