(R)-4-(tert-Butyl)-2-(5-chloropyridin-2-yl)-4,5-dihydrooxazole

97%, 99%e.e.

Reagent Code: #232159
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CAS Number 2757083-24-0

science Other reagents with same CAS 2757083-24-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.717 g/mol
Formula C₁₂H₁₅ClN₂O
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 structural features make it valuable in asymmetric synthesis, where the oxazole ring and chiral center contribute to high enantioselectivity in catalytic reactions. Commonly employed in the development of kinase inhibitors and receptor modulators due to its ability to enhance binding affinity and metabolic stability. Also utilized in agrochemical research for designing novel pesticides with improved environmental profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,660.00
inventory 250mg
10-20 days ฿18,110.00

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(R)-4-(tert-Butyl)-2-(5-chloropyridin-2-yl)-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 structural features make it valuable in asymmetric synthesis, where the oxazole ring and chiral center contribute to high enantioselectivity in catalytic reactions. Commonly employed in the development of kinase inhibitors and receptor modulators due to its ability to enhance binding affinity and metabolic stability. Also utilized in agrochem

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its structural features make it valuable in asymmetric synthesis, where the oxazole ring and chiral center contribute to high enantioselectivity in catalytic reactions. Commonly employed in the development of kinase inhibitors and receptor modulators due to its ability to enhance binding affinity and metabolic stability. Also utilized in agrochemical research for designing novel pesticides with improved environmental profiles.

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