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Trifluorovinylphosphonic difluoride, also known as (CF3)2P(O)F2, is a chemical compound that belongs to the class of organophosphorus compounds. It is a colorless liquid with a pungent odor and is highly reactive due to the presence of the phosphonic group and multiple fluorine atoms. trifluorovinylphosphonic difluoride is primarily used as a reagent in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals, where it serves as a fluorinating agent or a precursor to other organophosphorus compounds. Due to its reactivity and potential toxicity, it is essential to handle trifluorovinylphosphonic difluoride with proper safety measures and in a controlled environment.

58734-90-0

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58734-90-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58734-90-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,7,3 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58734-90:
(7*5)+(6*8)+(5*7)+(4*3)+(3*4)+(2*9)+(1*0)=160
160 % 10 = 0
So 58734-90-0 is a valid CAS Registry Number.

58734-90-0Downstream Products

58734-90-0Relevant academic research and scientific papers

Inorganic chemistry of fluorocarbenes. 1. Reactions of tetrafluoroethylidene with fluorine-containing phosphines

Sharp, Kenneth G.,Schwager, Irving

, p. 1697 - 1701 (1976)

The interactions of tetrafluoroethylidene with three fluorine-containing phosphines have been investigated. The source of the carbene is the pyrolytic decomposition of C2F5SiF3 at 200°C. The reaction of CF3CF with PF3 generates CF2=CFPF4 and PF5; reaction with (CF3)3P leads to (CF3)2PCF(CF3)2; and reaction with (CF3)2PCF(CF3)2 produces the fluorocarbon (CF3)2CFCF(CF3)2. The possibility that the vinylphosphorane product of the PF3 reaction results from fluorine-transfer rearrangement of C2F5PF2 as an intermediate product was discredited by a demonstration that C2F5PF2 is thermally stable under the reaction conditions. Other mechanistic pathways are discussed.

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