83558-76-3 Usage
Description
Hexafluoro-2,2-diphenylpropane is a synthetic organofluorine compound, characterized by its solid, white crystalline form at room temperature. It features a unique molecular structure with two phenyl rings attached to a three-carbon chain, and six fluorine atoms bonded to the central carbon atom. Known for its high stability and resistance to heat and chemical reactions, this specialized fluorocarbon is widely used in the production of plastics, resins, and coatings.
Uses
Used in Plastics Industry:
Hexafluoro-2,2-diphenylpropane is used as a key component in the manufacturing of high-performance plastics due to its exceptional stability and resistance to heat and chemical reactions. This makes the resulting plastics suitable for applications requiring durability and resistance to harsh conditions.
Used in Resin Production:
In the resin industry, hexafluoro-2,2-diphenylpropane serves as an essential ingredient for creating resins with enhanced properties. Its incorporation into resins improves their heat and chemical resistance, making them ideal for use in various industrial applications.
Used in Coating Formulation:
Hexafluoro-2,2-diphenylpropane is utilized as a critical component in the formulation of coatings, providing them with superior heat and chemical resistance. This makes the coatings ideal for use in environments where they are exposed to high temperatures and corrosive substances, ensuring long-lasting protection and durability.
Check Digit Verification of cas no
The CAS Registry Mumber 83558-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,5 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83558-76:
(7*8)+(6*3)+(5*5)+(4*5)+(3*8)+(2*7)+(1*6)=163
163 % 10 = 3
So 83558-76-3 is a valid CAS Registry Number.
83558-76-3Relevant articles and documents
Process for preparing 2,2-diphenylhexafluoropropanes
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, (2008/06/13)
2,2-diphenylhexafluoropropanes are prepared by condensation reaction of benzene or benzenes substituted with a halogen atom or atoms, a lower alkyl group or groups or a hydroxyl group or groups with hexafluoroacetone in the presence of trifluoromethane sulfonic acid. Among the 2,2-diphenylhexafluoropropanes, 2,2-diphenylhexafluoropropane and 2,2-bis(p-chlorophenyl)hexafluoropropane are novel compounds.
