2570984-82-4 Usage
Description
(S)-2-(6-benzhydrylpyridin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole is a complex chemical compound characterized by its unique molecular structure. It features a pyridine ring with a benzhydryl group attached, a tert-butyl group, and a dihydrooxazole ring. As a chiral molecule, it has a specific spatial arrangement of atoms, leading to the existence of two enantiomers with distinct biological activities. (S)-2-(6-benzhydrylpyridin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole holds potential for applications in medicinal chemistry, particularly in the development of new drugs for various diseases, and its molecular structure suggests it may possess unique physicochemical properties of interest for further research and development in organic chemistry.
Uses
Used in Medicinal Chemistry:
(S)-2-(6-benzhydrylpyridin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole is used as a key component in the development of novel drugs for the treatment of various diseases. Its unique molecular structure and chiral properties make it a promising candidate for creating new pharmaceuticals with specific therapeutic effects.
Used in Organic Chemistry Research:
In the field of organic chemistry, (S)-2-(6-benzhydrylpyridin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole is used as a subject of study to explore its unique physicochemical properties. This research could lead to advancements in understanding molecular interactions and the development of new synthetic methods or applications in material science.
Used in Pharmaceutical Industry:
(S)-2-(6-benzhydrylpyridin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole is used as a building block or intermediate in the synthesis of complex pharmaceutical compounds. Its chiral nature and structural diversity make it valuable for creating innovative drugs with improved efficacy and selectivity.
Used in Drug Design and Development:
(S)-2-(6-benzhydrylpyridin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole is used as a template in drug design and development, particularly for targeting specific biological pathways or receptors. Its unique structure may allow for the creation of drugs with fewer side effects and higher specificity towards their intended targets.
Check Digit Verification of cas no
The CAS Registry Mumber 2570984-82-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 2,5,7,0,9,8 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2570984-82:
(9*2)+(8*5)+(7*7)+(6*0)+(5*9)+(4*8)+(3*4)+(2*8)+(1*2)=214
214 % 10 = 4
So 2570984-82-4 is a valid CAS Registry Number.
2570984-82-4Relevant articles and documents
Efficient Synthesis of Bulky 2,2’-Bipyridine and (S)-Pyridine-Oxazoline Ligands
Zheng, Zhipeng,Walsh, Patrick J.
supporting information, p. 800 - 807 (2020/12/01)
Bulky N,N’-bidentate ligands can furnish catalysts with enhanced catalytic activity compared to commercially available ligands. Straightforward methods to effectively synthesize a broad range of these ligands, however, are uncommon. In this work, a simple and efficient method is developed for the synthesis of bulky N,N’-bidentate ligands, including 2,2’-bipyridines and enantioenriched pyridine-oxazolines. The Pd/NIXANTPHOS catalyst system enabled synthesis of a series of bulky 2,2’-bipyridine-based ligands and (S)-pyridine oxazoline-based enantioenriched ligands with good to excellent yields. The ligands have been benchmarked in the aminofluorination of styrene. (Figure presented.).
