7-Bromo-3,3-dimethyl-2,3-dihydropyrazolo[5,1-b]oxazole

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Reagent Code: #142251
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CAS Number 2676863-02-6

science Other reagents with same CAS 2676863-02-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.06 g/mol
Formula C₇H₉BrN₂O
thermostat Physical Properties
Boiling Point 272.1±28.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.71±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of bioactive compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting inflammatory diseases and cancer. Its bromo-functionalized heterocyclic structure allows for further cross-coupling reactions, enabling rapid diversification in drug discovery programs. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿10,660.00
inventory 100mg
10-20 days ฿17,060.00
inventory 250mg
10-20 days ฿34,140.00

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7-Bromo-3,3-dimethyl-2,3-dihydropyrazolo[5,1-b]oxazole
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Used as a key intermediate in the synthesis of bioactive compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting inflammatory diseases and cancer. Its bromo-functionalized heterocyclic structure allows for further cross-coupling reactions, enabling rapid diversification in drug discovery programs. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

Used as a key intermediate in the synthesis of bioactive compounds, particularly in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting inflammatory diseases and cancer. Its bromo-functionalized heterocyclic structure allows for further cross-coupling reactions, enabling rapid diversification in drug discovery programs. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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