7-Bromo-2H-1,4-benzoxazin-3(4H)-one

95%

Reagent Code: #144259
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CAS Number 321436-06-0

science Other reagents with same CAS 321436-06-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.04 g/mol
Formula C₈H₆BrNO₂
thermostat Physical Properties
Boiling Point 381.5±42.0 °C(Predicted)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents and antipsychotic drugs. Its structure allows for selective modifications at the 7-position, making it valuable in medicinal chemistry for creating derivatives with enhanced biological activity. Commonly employed in ring-expansion reactions and cross-coupling processes to build complex heterocyclic systems found in bioactive molecules. Also utilized in research settings for designing novel drug candidates targeting neurological disorders.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,120.00
inventory 5g
10-20 days ฿4,480.00
inventory 10g
10-20 days ฿7,040.00
inventory 100g
10-20 days ฿53,280.00
inventory 25g
10-20 days ฿15,360.00

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7-Bromo-2H-1,4-benzoxazin-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 antipsychotic drugs. Its structure allows for selective modifications at the 7-position, making it valuable in medicinal chemistry for creating derivatives with enhanced biological activity. Commonly employed in ring-expansion reactions and cross-coupling processes to build complex heterocyclic systems found in bioactive molecules. Also utilized in research setting

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents and antipsychotic drugs. Its structure allows for selective modifications at the 7-position, making it valuable in medicinal chemistry for creating derivatives with enhanced biological activity. Commonly employed in ring-expansion reactions and cross-coupling processes to build complex heterocyclic systems found in bioactive molecules. Also utilized in research settings for designing novel drug candidates targeting neurological disorders.

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