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Atomfair 3-(Bicyclo[2.2.1]hept-5-EN-2-YL)-1,1,1-trifluoro-2-(trifluoromethyl)propan-2-OL C11H12F6O CAS 196314-61-1
3-(Bicyclo[2.2.1]hept-5-EN-2-YL)-1,1,1-trifluoro-2-(trifluoromethyl)propan-2-OL (CAS: 196314-61-1) is a high-purity fluorinated organic compound with the molecular formula C11H12F6O . This specialized chemical features a bicyclo[2.2.1]heptene core functionalized with a hexafluoropropanol group, making it a valuable intermediate for advanced synthetic applications. Its unique structure combines steric hindrance and electron-withdrawing trifluoromethyl groups, enhancing reactivity in selective transformations. Ideal for pharmaceutical, agrochemical, and materials science research, this compound is rigorously tested for consistency (≥95% purity by HPLC/GC) and supplied in sealed, light-resistant packaging under inert gas to ensure stability. Compatible with organometallic catalysis and fluorination reactions, it is a versatile building block for novel fluorinated scaffolds.
Description
3-(Bicyclo[2.2.1]hept-5-EN-2-YL)-1,1,1-trifluoro-2-(trifluoromethyl)propan-2-OL (CAS: 196314-61-1) is a high-purity fluorinated organic compound with the molecular formula C11H12F6O. This specialized chemical features a bicyclo[2.2.1]heptene core functionalized with a hexafluoropropanol group, making it a valuable intermediate for advanced synthetic applications. Its unique structure combines steric hindrance and electron-withdrawing trifluoromethyl groups, enhancing reactivity in selective transformations. Ideal for pharmaceutical, agrochemical, and materials science research, this compound is rigorously tested for consistency (≥95% purity by HPLC/GC) and supplied in sealed, light-resistant packaging under inert gas to ensure stability. Compatible with organometallic catalysis and fluorination reactions, it is a versatile building block for novel fluorinated scaffolds.
Properties
- CAS Number: 196314-61-1
- Complexity: 342
- IUPAC Name: 2-(2-bicyclo[2.2.1]hept-5-enylmethyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol
- InChI: InChI=1S/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
- InChI Key: NIQLOLNJWXWZHX-UHFFFAOYSA-N
- Exact Mass: 274.07923397
- Molecular Formula: C11H12F6O
- Molecular Weight: 274.20
- SMILES: C1C2CC(C1C=C2)CC(C(F)(F)F)(C(F)(F)F)O
- Topological: 20.2
- Monoisotopic Mass: 274.07923397
- Synonyms: 196314-61-1, 3-(BICYCLO[2.2.1]HEPT-5-EN-2-YL)-1,1,1-TRIFLUORO-2-(TRIFLUOROMETHYL)PROPAN-2-OL, 2-(Bicyclo[2.2.1]hept-5-en-2-ylmethyl)-1,1,1,3,3,3-hexafluoropropan-2-ol, 2-(2-bicyclo[2.2.1]hept-5-enylmethyl)-1,1,1,3,3,3-hexafluoropropan-2-ol, 2-({bicyclo[2.2.1]hept-5-en-2-yl}methyl)-1,1,1,3,3,3-hexafluoropropan-2-ol, 2-[(Bicyclo[2.2.1]hept-5-en-2-yl)methyl]-1,1,1,3,3,3-hexafluoropropan-2-ol, NIQLOLNJWXWZHX-UHFFFAOYSA-N, SCHEMBL75457, DTXSID30612716, 2-(Bicyclo[2.2.1]hept-5-en-2-yl)-1,1,1-trifluoro-2-(trifluoromethyl)propan-2-ol, AKOS022193586, GS-0002, CS-0449534, G73687, Bicyclo[2.2.1]hept-5-ene-2-ethanol, a,a-bis(trifluoromethyl)-, Bicyclo[2.2.1]hept-5-ene-2-ethanol, .alpha.,.alpha.-bis(trifluoromethyl)-, (1S,4S)
This compound serves as a key synthon in the synthesis of fluorinated pharmaceuticals, leveraging its bicyclic and trifluoromethyl motifs for bioactivity modulation. It is employed in asymmetric catalysis to construct chiral fluorinated intermediates for drug discovery. Researchers also utilize it in polymer science to develop high-performance fluoropolymers with enhanced thermal and chemical resistance. Its electron-deficient nature makes it suitable for studying non-covalent interactions in supramolecular chemistry.
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