3-(3-Bromo-1,2-oxazol-5-yl)pyridine

≥95%

Reagent Code: #149877
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CAS Number 1159976-79-0

science Other reagents with same CAS 1159976-79-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.04 g/mol
Formula C₈H₅BrN₂O
badge Registry Numbers
MDL Number MFCD04035590
thermostat Physical Properties
Boiling Point 350.3±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.605±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in agrochemical research for designing novel pesticides with improved environmental stability and mode of action. Commonly utilized in medicinal chemistry for scaffold modification to optimize pharmacokinetic properties in drug candidates.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿10,450.00
inventory 250mg
10-20 days ฿31,260.00

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3-(3-Bromo-1,2-oxazol-5-yl)pyridine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in agrochemical research for designing novel pesticides with improved environmental stability and mode of action. Commonly utilized in medicinal chemistry for scaffold modification to optimize pharmacokinetic properties in drug candidates.
Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in agrochemical research for designing novel pesticides with improved environmental stability and mode of action. Commonly utilized in medicinal chemistry for scaffold modification to optimize pharmacokinetic properties in drug candidates.
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