1997306-77-0 Usage
Description
(4S,5S)-4,5-diphenyl-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole is a chiral chemical compound with the molecular formula C22H18F3NO. It is a dihydrooxazole derivative that features two phenyl groups and a trifluoromethylpyridin-2-yl group. (4S,5S)-4,5-diphenyl-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole is characterized by its (4S,5S) configuration, which is significant in the field of stereochemistry.
Uses
Used in Organic Synthesis:
(4S,5S)-4,5-diphenyl-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole is utilized as a building block in organic synthesis, providing a structural foundation for the creation of more complex molecules. Its unique arrangement of functional groups allows for versatile chemical reactions and the formation of a variety of compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4S,5S)-4,5-diphenyl-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole is employed as a potential precursor for drug development. Its specific stereochemistry and functional groups may contribute to the design of new pharmaceuticals with targeted biological activities.
Used in Research:
(4S,5S)-4,5-diphenyl-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole is also used in research settings to explore its unique structural features and potential biological activity. Researchers are interested in understanding how this compound interacts with biological systems, which could lead to the discovery of new therapeutic agents or insights into molecular recognition processes.
Check Digit Verification of cas no
The CAS Registry Mumber 1997306-77-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,9,9,7,3,0 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1997306-77:
(9*1)+(8*9)+(7*9)+(6*7)+(5*3)+(4*0)+(3*6)+(2*7)+(1*7)=240
240 % 10 = 0
So 1997306-77-0 is a valid CAS Registry Number.
1997306-77-0Relevant articles and documents
Palladium-Catalyzed Enantioselective Redox-Relay Heck Arylation of 1,1-Disubstituted Homoallylic Alcohols
Chen, Zhi-Min,Hilton, Margaret J.,Sigman, Matthew S.
supporting information, p. 11461 - 11464 (2016/10/06)
An enantioselective redox-relay oxidative Heck arylation of 1,1-disubstituted alkenes to construct β-stereocenters was developed using a new pyridyl-oxazoline ligand. Various 1,2-diaryl carbonyl compounds were readily obtained in moderate yield and good to excellent enantioselectivity. Additionally, analysis of the reaction outcomes using multidimensional correlations revealed that enantioselectivity is tied to specific electronic features of the 1,1-disubstituted alkenol and the extent of polarizability of the ligand.
