(S)-2-(5-Bromopyridin-2-yl)-4-isopropyl-4,5-dihydrooxazole

97%, 99% e.e.

Reagent Code: #233249
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CAS Number 2757083-25-1

science Other reagents with same CAS 2757083-25-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.14 g/mol
Formula C₁₁H₁₃BrN₂O
thermostat Physical Properties
Boiling Point 338.5±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.50±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in the production of pharmaceuticals targeting central nervous system disorders. Its structural features make it valuable in asymmetric synthesis, where it helps introduce chirality in drug molecules. Commonly employed in the development of kinase inhibitors and neuroactive agents due to its ability to enhance selectivity and binding affinity. Also utilized in agrochemical research for creating enantiomerically pure herbicides and pesticides. Its bromine functionality allows for further cross-coupling reactions, enabling diverse molecular modifications in medicinal chemistry campaigns.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,340.00
inventory 250mg
10-20 days ฿22,650.00

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(S)-2-(5-Bromopyridin-2-yl)-4-isopropyl-4,5-dihydrooxazole
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Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in the production of pharmaceuticals targeting central nervous system disorders. Its structural features make it valuable in asymmetric synthesis, where it helps introduce chirality in drug molecules. Commonly employed in the development of kinase inhibitors and neuroactive agents due to its ability to enhance selectivity and binding affinity. Also utilized in agrochemical research for creating enantiomerica

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in the production of pharmaceuticals targeting central nervous system disorders. Its structural features make it valuable in asymmetric synthesis, where it helps introduce chirality in drug molecules. Commonly employed in the development of kinase inhibitors and neuroactive agents due to its ability to enhance selectivity and binding affinity. Also utilized in agrochemical research for creating enantiomerically pure herbicides and pesticides. Its bromine functionality allows for further cross-coupling reactions, enabling diverse molecular modifications in medicinal chemistry campaigns.

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