106760-61-6 Usage
Description
(R)-2-phenyloxetane, with the molecular formula C8H10O, is a chemical compound featuring a six-membered ring that includes an oxygen atom and a phenyl (C6H5) group. As an enantiomer of 2-phenyloxetane, it exists in two non-superimposable mirror-image forms. (R)-2-phenyloxetane has garnered interest for its potential applications in organic synthesis and as a precursor for constructing other compounds. Additionally, it is being explored for its pharmaceutical potential, with ongoing research into its biological activity and possible therapeutic applications. As a relatively novel and less extensively studied chemical, further investigation is required to comprehensively understand its characteristics and utility across different sectors.
Uses
Used in Organic Synthesis:
(R)-2-phenyloxetane is used as a building block in the synthesis of various organic compounds due to its unique structure and reactivity. Its ability to form different chemical bonds and participate in numerous reactions makes it a valuable component in creating a wide range of molecules.
Used in Pharmaceutical Applications:
(R)-2-phenyloxetane is being investigated for its potential as a pharmaceutical agent, with research focusing on its biological activity and possible therapeutic uses. Its unique structure and properties may offer new avenues for drug development, particularly in the treatment of various diseases and conditions.
Used in Chemical Research:
As a less commonly studied compound, (R)-2-phenyloxetane serves as a subject of interest for chemical research. Its exploration can contribute to the broader understanding of chemical properties, reactivity, and potential applications in various fields, including materials science, environmental chemistry, and more.
Check Digit Verification of cas no
The CAS Registry Mumber 106760-61-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,6 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106760-61:
(8*1)+(7*0)+(6*6)+(5*7)+(4*6)+(3*0)+(2*6)+(1*1)=116
116 % 10 = 6
So 106760-61-6 is a valid CAS Registry Number.
106760-61-6Relevant articles and documents
Ultrafast Iron-Catalyzed Reduction of Functionalized Ketones: Highly Enantioselective Synthesis of Halohydrines, Oxaheterocycles, and Aminoalcohols
Blasius, Clemens K.,Vasilenko, Vladislav,Gade, Lutz H.
supporting information, p. 10231 - 10235 (2018/07/31)
A molecularly defined chiral boxmi iron alkyl complex catalyzes the hydroboration of various functionalized ketones and provides the corresponding chiral halohydrines, oxaheterocycles (oxiranes, oxetanes, tetrahydrofurans, and dioxanes) and amino alcohols with excellent enantioselectivities (up to >99 %ee) and conversion efficiencies at low catalyst loadings (as low as 0.5 mol %). Turnover frequencies of greater than 40000 h?1 at ?30 °C highlight the activity of this earth-abundant metal catalyst which tolerates a large number of functional groups.
2-Lithiated-2-phenyloxetane: A new attractive synthon for the preparation of oxetane derivatives
Coppi, Donato Ivan,Salomone, Antonio,Perna, Filippo Maria,Capriati, Vito
scheme or table, p. 9918 - 9920 (2011/10/09)
A valuable and direct method to access 2-substituted-2-phenyloxetanes by electrophilic quenching of the corresponding 2-lithiated derivative has, for the first time, been described. 2-Lithiated-2-phenyloxetane was found to be configurationally unstable. E
Applications of planar-chiral heterocycles in enantioselective catalysis: Cu(I)/bisazaferrocene-catalyzed asymmetric ring expansion of oxetanes to tetrahydrofurans
Lo, Michael M.-C.,Fu, Gregory C.
, p. 2621 - 2634 (2007/10/03)
A planar-chiral, C2-symmetric bisazaferrocene ligand is shown to control the stereochemistry of Cu(I)-catalyzed ring expansions of oxetanes to tetrahydrofurans.
