(S)-4-(tert-Butyl)-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole

98%

Reagent Code: #57570
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CAS Number 1257527-14-2

science Other reagents with same CAS 1257527-14-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.27 g/mol
Formula C₁₃H₁₅F₃N₂O
thermostat Physical Properties
Melting Point 56-59 °C
Boiling Point 335.7±42.0 °C
inventory_2 Storage & Handling
Density 1.25±0.1 g/cm3
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. It plays a significant role in the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals, agrochemicals, and fine chemicals. Its structure, featuring a dihydrooxazole ring and a trifluoromethylpyridine moiety, enhances its ability to induce stereoselectivity in various catalytic processes, such as hydrogenation, cyclopropanation, and carbon-carbon bond formation. Additionally, its tert-butyl group contributes to increased stability and steric hindrance, making it effective in controlling the spatial arrangement of reactants during synthesis. This chemical is also explored in material science for designing advanced chiral materials with potential applications in optoelectronics and sensors.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,892.00

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(S)-4-(tert-Butyl)-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. It plays a significant role in the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals, agrochemicals, and fine chemicals. Its structure, featuring a dihydrooxazole ring and a trifluoromethylpyridine moiety, enhances its ability to induce stereoselectivity in various catalytic processes, such as hydrogenation, cyclop

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. It plays a significant role in the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals, agrochemicals, and fine chemicals. Its structure, featuring a dihydrooxazole ring and a trifluoromethylpyridine moiety, enhances its ability to induce stereoselectivity in various catalytic processes, such as hydrogenation, cyclopropanation, and carbon-carbon bond formation. Additionally, its tert-butyl group contributes to increased stability and steric hindrance, making it effective in controlling the spatial arrangement of reactants during synthesis. This chemical is also explored in material science for designing advanced chiral materials with potential applications in optoelectronics and sensors.

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