121680-77-1 Usage
Description
(R)-(+)-2,3,4,5,6-PENTAFLUOROSTYRENE OXIDE, with the chemical formula C8H3F5O, is a colorless liquid characterized by a distinct odor. It is insoluble in water and is recognized for its high reactivity, which allows it to participate in a variety of chemical reactions. This makes it a valuable building block in the synthesis of new compounds and materials, particularly in the production of specialty polymers and copolymers, as well as in the creation of pharmaceuticals and agrochemicals.
Uses
Used in Specialty Polymers and Copolymers Production:
(R)-(+)-2,3,4,5,6-PENTAFLUOROSTYRENE OXIDE is used as a monomer for the production of specialty polymers and copolymers. Its high reactivity and unique chemical structure contribute to the development of materials with specific properties tailored for various applications.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, (R)-(+)-2,3,4,5,6-PENTAFLUOROSTYRENE OXIDE is used as a key intermediate in the synthesis of various pharmaceuticals. Its ability to undergo multiple chemical reactions enables the creation of complex drug molecules with potential therapeutic benefits.
Used in Agrochemicals Production:
(R)-(+)-2,3,4,5,6-PENTAFLUOROSTYRENE OXIDE also finds application in the agrochemical sector, where it is utilized in the synthesis of compounds for pest control and crop protection. Its versatility in chemical reactions allows for the development of effective and targeted agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 121680-77-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,8 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121680-77:
(8*1)+(7*2)+(6*1)+(5*6)+(4*8)+(3*0)+(2*7)+(1*7)=111
111 % 10 = 1
So 121680-77-1 is a valid CAS Registry Number.
121680-77-1Relevant articles and documents
An efficient catalyst for asymmetric epoxidation of terminal olefins
Collman, James P.,Wang, Zhong,Straumanis, Andrei,Quelquejeu, Mélanie,Rose, Eric
, p. 460 - 461 (2007/10/03)
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Synthesis of Chiral Bitetralin-strapped "Twin Coronet" Porphyrins. Catalytic and Asymmetric Epoxidation of Styrene Derivatives
Naruta, Yoshinori,Ishihara, Nobuo,Tani, Fumito,Maruyama, Kazuhiro
, p. 1933 - 1936 (2007/10/02)
"Twin-coronet" porphyrins bearing optically active 1,1'-bitetrahydronaphthalene derivatives on the both faces of the porphyrin were prepared as enantioselective oxidation catalysts modeling on cytochrome P-450s.The eclipsed isomer of the corresponding iron(III) porphyrins catalyzed epoxidation of styrenes substituted with electron-withdrawing groups in high e.e. (61-89 percent) and high product selectivity.
