(S)-2-(5-Bromopyridin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole

97%, 99%ee

Reagent Code: #233257
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CAS Number 2757083-26-2

science Other reagents with same CAS 2757083-26-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.16 g/mol
Formula C₁₂H₁₅BrN₂O
thermostat Physical Properties
Boiling Point 345.1±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.41±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders. Its oxazole ring and bromopyridine moiety enable selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex molecules. The stereochemistry at the 4-position enhances enantioselectivity in asymmetric synthesis, useful in creating single-enantiomer drugs. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,500.00
inventory 250mg
10-20 days ฿19,500.00

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(S)-2-(5-Bromopyridin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders. Its oxazole ring and bromopyridine moiety enable selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex molecules. The stereochemistry at the 4-position enhances enantioselectivity in asymmetric synthesis, useful in creating single-enantiomer drugs. Also employed in agrochemical resea

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds targeting central nervous system disorders. Its oxazole ring and bromopyridine moiety enable selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex molecules. The stereochemistry at the 4-position enhances enantioselectivity in asymmetric synthesis, useful in creating single-enantiomer drugs. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles.

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