63863-43-4 Usage
Description
METHYL PERFLUORO(5-METHYL-4,7-DIOXANON-8-ENOATE) is a perfluorinated chemical compound characterized by its complex structure and the presence of carbon-fluorine bonds. These bonds are known for their strong and stable nature, contributing to the compound's resistance to heat, oil, and water. This property makes it a candidate for various industrial applications and consumer goods production.
Uses
Used in Industrial Applications:
METHYL PERFLUORO(5-METHYL-4,7-DIOXANON-8-ENOATE) is used as a key component in the production of various industrial products due to its heat, oil, and water resistance properties. This makes it suitable for applications where durability and stability are required.
Used in Consumer Goods Production:
METHYL PERFLUORO(5-METHYL-4,7-DIOXANON-8-ENOATE) is used as a raw material in the manufacturing of consumer goods, leveraging its stable and resistant characteristics to enhance the performance and longevity of the final products.
Check Digit Verification of cas no
The CAS Registry Mumber 63863-43-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,6 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63863-43:
(7*6)+(6*3)+(5*8)+(4*6)+(3*3)+(2*4)+(1*3)=144
144 % 10 = 4
So 63863-43-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H3F13O4/c1-24-4(23)5(13,14)8(19,20)26-6(15,7(16,17)18)9(21,22)25-3(12)2(10)11/h1H3
63863-43-4Relevant articles and documents
Process for producing fluorinated vinyl ether
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Page 6, (2008/06/13)
There is provided a process for producing a fluorinated vinyl ether from a fluorinated acid fluoride compound having an ester group as a precursor of a carboxylic acid group, or a SO2F group as a precursor of a sulfonic acid group, in high yield by simple operations. Said process is a production process comprising pyrolyzing a carboxylic acid potassium salt with a specific structure represented by the following formula in the absence of a solvent and/or while maintaining the salt in the solid state: wherein X is —CO2R or —SO2F, and R is an alkyl group.
Alkyl perfluoro-ω-fluoroformyl esters and their preparation
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, (2008/06/13)
Alkyl perfluoro-ω-fluoroformyl esters are provided which have the formula: STR1 wherein R is alkyl of 1-6 carbon atoms, and n is 0-6 (preferably 0). Compounds where n is 0 are prepared by contacting SO3 with a compound of the formula ROOC--CF2 --CF2 --OR1. Compounds where n is 1-6 are prepared by contacting a compound where n is 0 with hexafluoropropylene oxide.