(R)-2-(4-Methoxy-6-methylpyridin-2-yl)-4-phenyl-4,5-dihydrooxazole

98%

Reagent Code: #231398
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CAS Number 2757082-89-4

science Other reagents with same CAS 2757082-89-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.31 g/mol
Formula C₁₆H₁₆N₂O₂
inventory_2 Storage & Handling
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 pharmaceuticals targeting central nervous system disorders. Its oxazoline core with defined stereochemistry enables high enantioselectivity in catalytic reactions, making it valuable in asymmetric synthesis. Employed in the development of novel kinase inhibitors and anti-inflammatory agents due to its ability to modulate specific enzyme activities. Also utilized in agrochemical research for designing enantiomerically pure herbicides and pesticides with improved environmental profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,670.00

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(R)-2-(4-Methoxy-6-methylpyridin-2-yl)-4-phenyl-4,5-dihydrooxazole
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Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its oxazoline core with defined stereochemistry enables high enantioselectivity in catalytic reactions, making it valuable in asymmetric synthesis. Employed in the development of novel kinase inhibitors and anti-inflammatory agents due to its ability to modulate specific enzyme activities. Also utilized in agrochemical research for designing enan

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its oxazoline core with defined stereochemistry enables high enantioselectivity in catalytic reactions, making it valuable in asymmetric synthesis. Employed in the development of novel kinase inhibitors and anti-inflammatory agents due to its ability to modulate specific enzyme activities. Also utilized in agrochemical research for designing enantiomerically pure herbicides and pesticides with improved environmental profiles.

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