1079392-85-0 Usage
Uses
Used in Medicinal Chemistry:
(1R)-(6-hydroxyquinolin-4-yl)(8-vinylquinuclidin-2-yl)methyl 3,5-di(trifluoromethyl)benzoate is used as a pharmacological agent for its potential medicinal properties. The hydroxyquinolin and vinylquinuclidin groups may contribute to its activity against various biological targets, making it a candidate for drug discovery and development.
Used in Drug Discovery:
In the field of drug discovery, (1R)-(6-hydroxyquinolin-4-yl)(8-vinylquinuclidin-2-yl)methyl 3,5-di(trifluoromethyl)benzoate is used as a lead compound. Its unique structure allows for further optimization and modification to enhance its therapeutic potential, targeting specific diseases or conditions.
Used in Materials Science:
(1R)-(6-hydroxyquinolin-4-yl)(8-vinylquinuclidin-2-yl)methyl 3,5-di(trifluoromethyl)benzoate is used as a component in the development of new materials. Its structural features may enable the creation of novel materials with specific properties, such as improved stability or unique optical characteristics, for use in various industries.
Used in Organic Synthesis:
In organic synthesis, (1R)-(6-hydroxyquinolin-4-yl)(8-vinylquinuclidin-2-yl)methyl 3,5-di(trifluoromethyl)benzoate is used as a building block or intermediate. Its benzoyl moiety and trifluoromethyl substituents can be leveraged to synthesize more complex molecules with desired properties for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1079392-85-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,9,3,9 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1079392-85:
(9*1)+(8*0)+(7*7)+(6*9)+(5*3)+(4*9)+(3*2)+(2*8)+(1*5)=190
190 % 10 = 0
So 1079392-85-0 is a valid CAS Registry Number.
1079392-85-0Relevant academic research and scientific papers
Organocatalytic Nitroaldol Reaction Associated with Deuterium-Labeling
Yamada, Tsuyoshi,Kuwata, Marina,Takakura, Ryoya,Monguchi, Yasunari,Sajiki, Hironao,Sawama, Yoshinari
, p. 637 - 641 (2017/12/13)
A deuterium-labeling reaction of nitroalkanes in deuterium oxide and the subsequent nitroaldol reaction have been accomplished under basic and organocatalytic conditions to provide the deuterium-labeled β-nitroalcohols in high yields and high deuterium contents. β-Deuterated β-nitroalcohols could be smoothly obtained from the reaction of nitroalkanes and various electrophiles using the easily-removal basic resin WA30. Furthermore, the asymmetric nitroaldol reaction using nitromethane and α-keto esters as electrophiles in the presence of a quinine-derived organocatalyst in deuterium oxide could provide the desired β-deuterated nitroalcohol derivatives with high enantioselectivities. (Figure presented.).
Enantioselective organocatalyzed Henry reaction with fluoromethyl ketones
Bandini, Marco,Sinisi, Riccardo,Umani-Ronchi, Achille
supporting information; experimental part, p. 4360 - 4362 (2009/03/12)
Remarkable generality in scope of new C9-benzoylcupreines bearing electron-withdrawing substituents for the nitroaldol condensation with fluoromethyl ketones is presented. Both tri- and difluoromethyl ketones provided excellent levels of stereoinduction (
