15453-10-8 Usage
General Description
Trifluoro(1,1,2,2,3,4,4-heptafluorobut-3-enyl)oxirane is a compound that is formed by the combination of a trifluoro(1,1,2,2,3,4,4-heptafluorobut-3-enyl) group with an oxirane molecule. This chemical is a fluorinated epoxide with a highly fluorinated alkyl group attached. It is used in various industrial applications such as in the production of specialty chemicals, pharmaceuticals, and as a building block for synthesis of other compounds. Trifluoro(1,1,2,2,3,4,4-heptafluorobut-3-enyl)oxirane is known for its high stability and low reactivity, making it a valuable compound in research and manufacturing processes. Its unique structure and properties make it a versatile compound with potential applications in diverse fields.
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.
