1450841-25-4 Usage
Uses
Used in Pharmaceutical Industry:
2,6-Bis[(2S,3S)-4-Methyl-5,5-diphenyloxazolidin-2-yl]pyridine is used as a chiral ligand for the synthesis of enantiomerically pure pharmaceutical compounds. Its ability to control the stereochemistry of chemical reactions ensures the production of desired enantiomers with specific biological activities, improving the efficacy and safety of drugs.
Used in Chemical Research:
In the field of chemical research, 2,6-Bis[(2S,3S)-4-Methyl-5,5-diphenyloxazolidin-2-yl]pyridine serves as a versatile and efficient ligand for various organic transformations. It is employed in asymmetric hydrogenation, allylic substitution, and cyclopropanation reactions, contributing to the development of new synthetic methodologies and the exploration of novel chemical reactions.
Used in Agrochemical Industry:
2,6-Bis[(2S,3S)-4-Methyl-5,5-diphenyloxazolidin-2-yl]pyridine is utilized as a chiral ligand in the synthesis of enantiomerically pure agrochemicals. Its role in controlling the stereochemistry of chemical reactions helps in the production of active ingredients with specific biological properties, enhancing the effectiveness and selectivity of agrochemicals.
Used in Material Science:
In material science, 2,6-Bis[(2S,3S)-4-Methyl-5,5-diphenyloxazolidin-2-yl]pyridine is employed as a chiral ligand for the synthesis of enantiomerically pure materials with unique properties. Its ability to control the stereochemistry of chemical reactions contributes to the development of advanced materials with specific optical, electronic, or mechanical properties.
Overall, 2,6-Bis[(2S,3S)-4-Methyl-5,5-diphenyloxazolidin-2-yl]pyridine is a versatile and efficient chiral ligand with a wide range of applications across various industries, including pharmaceuticals, chemical research, agrochemicals, and material science. Its ability to control the stereochemistry of chemical reactions makes it a valuable tool for the development of enantiomerically pure compounds and the advancement of synthetic methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 1450841-25-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,8,4 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1450841-25:
(9*1)+(8*4)+(7*5)+(6*0)+(5*8)+(4*4)+(3*1)+(2*2)+(1*5)=144
144 % 10 = 4
So 1450841-25-4 is a valid CAS Registry Number.
1450841-25-4Relevant academic research and scientific papers
Chiral Bis(oxazolidine)pyridine-copper-catalyzed enantioselective friedel-crafts alkylation of indoles with nitroalkenes
Sato, Toru,Arai, Takayoshi
, p. 349 - 354 (2014/03/21)
Catalytic asymmetric Friedel-Crafts reaction of indoles with nitroalkenes was catalyzed by the stereochemically tunable bis(oxazolidine)pyridine (PyBodine)-Cu(OTf)2 complex. Using the PyBodine(Val)-Cu(OTf) 2 catalyst gave the Friedel-Crafts ?adducts with highly enantioselective manner. For the 1,4-bis[(E)-2-nitrovinyl]benzene, the reaction proceeded in a meso-trick manner to give the chiral double Friedel-Crafts adduct with 97% enantiomeric excess. Georg Thieme Verlag Stuttgart New York.
