96250-37-2 Usage
Uses
Used in Polymer and Coating Industry:
2,2,3,3-TETRAFLUOROPROPYL 2-FLUOROACRYLATE is used as a monomer for the synthesis of fluorinated polymers, contributing to the development of materials with improved surface properties, such as resistance to heat, chemicals, and weathering. Its presence in these polymers enhances adhesion and durability, which is crucial for various applications in this industry.
Used in Medical Device Industry:
In the medical field, 2,2,3,3-TETRAFLUOROPROPYL 2-FLUOROACRYLATE is used as a component in the development of medical devices, leveraging its chemical stability and biocompatibility. Its resistance to degradation and ability to repel certain substances make it suitable for use in devices that require long-term performance and minimal maintenance.
Used in Electronics Industry:
2,2,3,3-TETRAFLUOROPROPYL 2-FLUOROACRYLATE is utilized in the electronics industry as a material for creating protective coatings and components that can withstand harsh environmental conditions. Its heat and chemical resistance are particularly beneficial in applications where electronic devices are exposed to extreme temperatures or corrosive substances.
Used in Optical Materials Industry:
2,2,3,3-TETRAFLUOROPROPYL 2-FLUOROACRYLATE is also used in the production of optical materials, where its stability and resistance to degradation are essential for maintaining the clarity and performance of optical components over time. Its use in this industry contributes to the development of high-quality lenses, filters, and other optical devices.
Check Digit Verification of cas no
The CAS Registry Mumber 96250-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,5 and 0 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96250-37:
(7*9)+(6*6)+(5*2)+(4*5)+(3*0)+(2*3)+(1*7)=142
142 % 10 = 2
So 96250-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H5F5O2/c1-3(7)4(12)13-2-6(10,11)5(8)9/h5H,1-2H2
96250-37-2Relevant academic research and scientific papers
REACTIONS OF HALOGEN FLUORIDES XII. REACTION OF BROMINE TRIFLUORIDE WITH BROMINE-CONTAINING ESTERS. A NEW METHOD FOR THE SYNTHESIS OF FLUOROALKYL 2-FLUOROACRYLATES
Kartashov, A. V.,Chuvatkin, N. N.,Boguslavskaya, L. S.
, p. 2243 - 2248 (2007/10/02)
Being weak Lewis bases, esters reduce the reactivity of bromine trifluoride in the substitutive fluorination of organic bromine derivatives.For this reason the rate of the reaction of bromine trifluoride with bromine-containing esters depends not only on the electronic characteristics of the substituents at the reaction center but also on the basicity of the ester.As a rule, the selectivity of the reaction increases with increase in the basicity of the ester.The reaction of bromine trifluoride or chlorine monofluoride with fluoroalkyl 2,3-dibromopropionates can be used successfully for the synthesis of monomers (fluoroalkyl 2-fluoroacrylates).
