375-62-2 Usage
Uses
Used in Specialty Chemicals and Materials Industry:
PERFLUOROPENTANOYL FLUORIDE 98 is used as a key building block for synthesizing fluorinated polymers and surfactants, which are valued for their specific chemical and physical properties. These synthesized compounds are crucial in developing high-performance materials with applications in various sectors.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, PERFLUOROPENTANOYL FLUORIDE 98 is utilized as an intermediate in the production of certain drugs. Its reactivity allows for the creation of complex molecular structures that can be tailored for specific medicinal purposes.
Used in Agrochemical Industry:
PERFLUOROPENTANOYL FLUORIDE 98 is used as a precursor in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products designed to enhance crop protection and yield.
Used in Electronic Materials Industry:
PERFLUOROPENTANOYL FLUORIDE 98 is also employed in the production of electronic materials, where its unique properties can be leveraged to create advanced components for the electronics industry, such as in the development of high-performance coatings or specialized materials for semiconductor manufacturing.
Given the high reactivity and potential health risks associated with PERFLUOROPENTANOYL FLUORIDE 98, it is imperative that it is handled with appropriate safety measures in place across all applications and industries where it is utilized.
Check Digit Verification of cas no
The CAS Registry Mumber 375-62-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 375-62:
(5*3)+(4*7)+(3*5)+(2*6)+(1*2)=72
72 % 10 = 2
So 375-62-2 is a valid CAS Registry Number.
InChI:InChI=1/C5F10O/c6-1(16)2(7,8)3(9,10)4(11,12)5(13,14)15
375-62-2Relevant academic research and scientific papers
Polyfluorinated ethers: IV.* By-products in the synthesis of polyfluorinated alkyl vinyl ethers in a solvating solvent
Yuminov
, p. 1715 - 1720 (2007/10/03)
By-products formed in the synthesis of perfluoro(propyl vinyl ether), perfluoro(2-propoxypropyl vinyl ether), and methyl perfluoro(4-vinyloxybutanoate) in a solvating solvent have been studied. 1998 MAHK "Hayka/Interperiodica".
THERMAL CONVERSIONS OF PERFLUOROALKYLVINYL ETHERS
Kartsov, S. V.,Yuminov, V. S.,Maksimov, V. L.
, p. 1252 - 1256 (2007/10/02)
Perfluoroalkylvinyl ethers RFOCF=CF2 are isomerized and oligomerized at 160-205 degC by a radical chain mechanism forming acid fluorides of the oligomeric perfluoro-alkoxycarboxylic acids RFF)>nCF2COF (n = 0-2) of two types, 'head-to-head' F)CF2CF2COF group> and 'head-to-trail' F)CF2COF group>.The ratio of these isomers is close to 2 irrespective of the structure of RF, the process temperature, and the molecular weight of the oligomer.
Halogen Mobility in SN2 Reactions of Carbonyl Compounds. Comparisons with Aromatic Halogen Mobility
Miller, Joseph,Ying, Oi-Ling
, p. 323 - 328 (2007/10/02)
Kinetic studies, using conductometric techniques, have been carried out for isopropanolysis (solvolysis) reactions of some alkanoyl, benzoyl and perfuoroalkanoyl halides, viz. butanoyl and benzoyl fluorides, chlorides,and bromides and perfluoropentanoyl fluoride and chloride.The halogen mobility orders, F N reactions at saturated and aromatic carbon, and have been discussed in mechanistic terms.The substrate class reactivity order is perfluoroalkanoyl >> benzoyl, alkanoyl.The actual ratios depend on which halogen is displaced, the ratios being larger on displacement of fluorine.
