7-Bromo-2,2-dimethyl-2H-benzo[b][1,4]oxazin-3(4H)-one

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Reagent Code: #140965
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CAS Number 934993-58-5

science Other reagents with same CAS 934993-58-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.1 g/mol
Formula C₁₀H₁₀NO₂Br
badge Registry Numbers
MDL Number MFCD18250285
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents and anxiolytic drugs. Its structure allows for selective modifications, making it valuable in medicinal chemistry for creating analogs with improved bioavailability and receptor selectivity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aryl or heteroaryl groups, enabling the construction of complex drug-like molecules. Also utilized in research settings for the development of novel benzoxazine derivatives with potential therapeutic activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,240.00
inventory 1g
10-20 days ฿24,010.00

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7-Bromo-2,2-dimethyl-2H-benzo[b][1,4]oxazin-3(4H)-one
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents and anxiolytic drugs. Its structure allows for selective modifications, making it valuable in medicinal chemistry for creating analogs with improved bioavailability and receptor selectivity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aryl or heteroaryl groups, enabling the construction of complex drug-like molecules. A

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents and anxiolytic drugs. Its structure allows for selective modifications, making it valuable in medicinal chemistry for creating analogs with improved bioavailability and receptor selectivity. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aryl or heteroaryl groups, enabling the construction of complex drug-like molecules. Also utilized in research settings for the development of novel benzoxazine derivatives with potential therapeutic activity.

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