196314-61-1 Usage
Uses
Used in Polymer Synthesis:
3-(BICYCLO[2.2.1]HEPT-5-EN-2-YL)-1,1,1-TRIFLUORO-2-(TRIFLUOROMETHYL)PROPAN-2-OL is used as a monomer in the production of fluorocarbon-based polymers. The presence of fluorinated groups in the molecule contributes to the unique properties of the resulting polymers, such as enhanced chemical stability, thermal resistance, and non-stick characteristics.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(BICYCLO[2.2.1]HEPT-5-EN-2-YL)-1,1,1-TRIFLUORO-2-(TRIFLUOROMETHYL)PROPAN-2-OL may be utilized as a building block for the development of novel drugs. Its unique structure and fluorinated groups can potentially be exploited to design new molecules with specific biological activities.
Used in Chemical Research:
3-(BICYCLO[2.2.1]HEPT-5-EN-2-YL)-1,1,1-TRIFLUORO-2-(TRIFLUOROMETHYL)PROPAN-2-OL can also be employed in chemical research as a starting material for the synthesis of various complex organic compounds. Its unique structure and functional groups make it a valuable tool for exploring new reaction pathways and developing innovative synthetic methods.
Used in Material Science:
In the field of material science, 3-(BICYCLO[2.2.1]HEPT-5-EN-2-YL)-1,1,1-TRIFLUORO-2-(TRIFLUOROMETHYL)PROPAN-2-OL may find applications in the development of advanced materials with specific properties. The incorporation of this molecule into polymer matrices or other materials could lead to the creation of new materials with improved performance characteristics, such as increased strength, durability, or resistance to environmental factors.
Check Digit Verification of cas no
The CAS Registry Mumber 196314-61-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,3,1 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 196314-61:
(8*1)+(7*9)+(6*6)+(5*3)+(4*1)+(3*4)+(2*6)+(1*1)=151
151 % 10 = 1
So 196314-61-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H12F6O/c12-10(13,14)9(18,11(15,16)17)5-8-4-6-1-2-7(8)3-6/h1-2,6-8,18H,3-5H2/t6-,7+,8?/m0/s1
196314-61-1Relevant academic research and scientific papers
Ishikawa, Takuji,Kodani, Tesuhiro,Yoshida, Tomohiro,Moriya, Tsukasa,Yamashita, Tsuneo,Toriumi, Minoru,Araki, Takayuki,Aoyama, Hirokazu,Hagiwara, Takuya,Furukawa, Takamitsu,Itani, Toshiro,Fujii, Kiyoshi
, p. 1791 - 1799 (2004)
We have synthesized various main-chain fluorinated polymers and studied base-resin properties, such as transparency at 157 nm, solubility in a standard alkaline developer, and lithographic performance. Main-chain-fluorinated polymers were synthesized by copolymerization of tetrafluoroethylene (TFE) with cyclic monomers, especially newly synthesized norbornene derivatives. We studied the correlation between pKa(OH) and the solubility of the copolymers of TFE and functional (fluoroalkyl alcohol group) norbornenes. Their solubility depends on the pKa value of the fluoroalkyl alcohol groups. We studied the impact of the polymerization initiators on base-resin properties. High transparency was obtained by using the fluorocarbon initiator. It was also confirmed that the monocyclic component improves dry-etch resistance and that fluorination at the terminal groups improves alkaline solubility. In addition, we found that the development characteristics of TFE/norbornene copolymers were significantly improved by the stereoselective (endo versus exo) partial protection of the hydroxyl groups in the fluoroalkyl alcohol moiety attached to norbornene unit. The polymer protected only in the exo position of the norbornene unit in the copolymer had a higher Rmax and a higher contrast. Positive-working resists based on these fluoropolymers were developed and 55 nm dense lines could be delineated by exposure at 157 nm wavelength with an alternating phase shift mask on a 0.9 NA 157 nm exposure tool. We have synthesized various main-chain fluorinated polymers and studied their transparency, dry-etch durability and solubility.
