27639-98-1 Usage
Description
PERFLUORO-2,5,8-TRIMETHYL-3,6,9-TRIOXADODECANOYL FLUORIDE is a complex organic compound characterized by its perfluorinated structure and multiple oxygen atoms. This molecule is known for its unique properties, such as high chemical stability and low surface tension, which make it suitable for various applications in different industries.
Uses
Used in Surfactant Industry:
PERFLUORO-2,5,8-TRIMETHYL-3,6,9-TRIOXADODECANOYL FLUORIDE is used as a precursor for the preparation of fluorinated imide salt compounds. These compounds are essential in the formulation of surfactants, which are widely used in various applications, including the production of detergents, wetting agents, and emulsifiers. The fluorinated nature of these compounds provides enhanced performance characteristics, such as improved stability and reduced environmental impact.
Used in Specialized Chemicals:
PERFLUORO-2,5,8-TRIMETHYL-3,6,9-TRIOXADODECANOYL FLUORIDE can also be utilized in the development of specialized chemicals for various industrial applications. Due to its unique chemical properties, it can be employed in the synthesis of materials with specific characteristics, such as high thermal stability, low friction, and excellent chemical resistance. These materials can be used in applications like lubricants, coatings, and sealants, where performance under extreme conditions is required.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the unique properties of PERFLUORO-2,5,8-TRIMETHYL-3,6,9-TRIOXADODECANOYL FLUORIDE may also make it a candidate for use in the pharmaceutical industry. Its chemical stability and low surface tension could potentially be harnessed in the development of drug delivery systems, targeting specific tissues or organs, or improving the bioavailability of certain medications.
Check Digit Verification of cas no
The CAS Registry Mumber 27639-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,6,3 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27639-98:
(7*2)+(6*7)+(5*6)+(4*3)+(3*9)+(2*9)+(1*8)=151
151 % 10 = 1
So 27639-98-1 is a valid CAS Registry Number.
InChI:InChI=1/C12F24O4/c13-1(37)2(14,6(19,20)21)38-11(33,34)4(17,8(25,26)27)40-12(35,36)5(18,9(28,29)30)39-10(31,32)3(15,16)7(22,23)24
27639-98-1Relevant articles and documents
Radical additions to fluoro-olefins. Photochemical mono-fluoroalkylation and sequential bis-fluoroalkylation of oxolane
Paleta, Oldrich,Cirkva, Vladimir,Kvicala, Jaroslav
, p. 125 - 134 (2007/10/03)
Oxolane was fluoroalkylated by its photoadditions under atmospheric pressure. Monofluoro-alkylations were carried out with hexafluoropropene (1) and perfluorovinyl ethers C3F7O-[CF(CF3)CF2O]n-CF=CF2 (2-4, n=0-2) by direct photoexcitation of the oleflns to give high yields of addition products 9-12 (81-94%). The reactions were completely regioselective at the oxolane molecule and almost completely regioselective (93-99%) at the double bond of fluoro-olefins; no bis-fluoroalkylated oxolanes were detected. The completely selective introduction of a second fluoroalkyl into position 5 of the oxolane molecule was accomplished by acetone-sensitised photoaddition of 2-fluoroalkylated oxolanes 9, 10 to fluoro-olefins 1 and 2. Byproducts from reactions of the dimethylketyl radical which is formed in the initiation step were isolated and have given some evidence about the reaction mechanism that is discussed.
