15453-10-8 Usage
Description
Trifluoro(1,1,2,2,3,4,4-heptafluorobut-3-enyl)oxirane is a fluorinated epoxide compound characterized by the attachment of a highly fluorinated heptafluorobut-3-enyl group to an oxirane molecule. This unique structure endows the compound with high stability and low reactivity, making it a valuable asset in research and manufacturing processes. Its versatility and potential applications across various fields highlight its significance in the chemical industry.
Uses
Used in Specialty Chemicals Production:
Trifluoro(1,1,2,2,3,4,4-heptafluorobut-3-enyl)oxirane serves as a key building block in the synthesis of specialty chemicals. Its unique fluorinated structure contributes to the development of high-performance materials with tailored properties for specific applications.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, trifluoro(1,1,2,2,3,4,4-heptafluorobut-3-enyl)oxirane is utilized as an intermediate in the synthesis of various drug molecules. Its fluorinated nature allows for the creation of novel compounds with improved pharmacokinetic and pharmacodynamic properties, enhancing their therapeutic efficacy.
Used in Material Science Research:
trifluoro(1,1,2,2,3,4,4-heptafluorobut-3-enyl)oxirane's high stability and low reactivity make it an attractive candidate for material science research. Trifluoro(1,1,2,2,3,4,4-heptafluorobut-3-enyl)oxirane can be employed in the development of new materials with unique properties, such as enhanced thermal stability, chemical resistance, or specific interactions with other molecules.
Used in Synthesis of Other Compounds:
Due to its versatile structure, trifluoro(1,1,2,2,3,4,4-heptafluorobut-3-enyl)oxirane is used as a starting material for the synthesis of other complex organic compounds. Its presence in the molecular framework can impart new functionalities and properties to the resulting compounds, expanding the scope of chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 15453-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,5 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15453-10:
(7*1)+(6*5)+(5*4)+(4*5)+(3*3)+(2*1)+(1*0)=88
88 % 10 = 8
So 15453-10-8 is a valid CAS Registry Number.
InChI:InChI=1/C6F10O/c7-1(2(8)9)3(10,11)4(12,13)5(14)6(15,16)17-5
15453-10-8Relevant articles and documents
SYNTHESIS OF OXYGEN-CONTAINING ORGANOFLUORINE COMPOUNDS AND THEIR REACTIONS XI. LIQUID-PHASE OXIDATION OF PERFLUORO-1,5-HEXADIENE BY ATMOSPHERIC OXYGEN
Filyakova, T. I.,Ilatovskii, R. E.,Zapevalov, A. Ya.
, p. 1818 - 1822 (2007/10/02)
The oxidation of perfluoro-1,5-hexadiene by atmospheric oxygen under UV irradiation gave perfluoro-1,5-hexadiene dioxide, 4,5-epoxyperfluorovaleryl fluoride, and perfluorosuccinyl fluoride.The intermediate oxidation product was 1,2-epoxyperfluoro-5-hexene.The obtained α-oxides undergo both nucleophilic and electrophilic opening of the epoxide ring, giving mono- and bifunctional derivatives.
