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

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Reagent Code: #244573
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CAS Number 1215325-65-7

science Other reagents with same CAS 1215325-65-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.14 g/mol
Formula C₉H₆F₃NO₂
badge Registry Numbers
MDL Number MFCD11840309
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structure supports the creation of potent bioactive molecules, especially in the design of antidepressants and antipsychotics. The electron-withdrawing trifluoromethyl group enhances metabolic stability and improves blood-brain barrier penetration, making it valuable in medicinal chemistry. Also employed in the preparation of selective enzyme inhibitors due to its rigid heterocyclic framework and favorable binding properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿43,440.00
100mg
10-20 days ฿12,990.00
250mg
10-20 days ฿21,780.00
7-(Trifluoromethyl)-2H-benzo[b][1,4]oxazin-3(4H)-one
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structure supports the creation of potent bioactive molecules, especially in the design of antidepressants and antipsychotics. The electron-withdrawing trifluoromethyl group enhances metabolic stability and improves blood-brain barrier penetration, making it valuable in medicinal chemistry. Also employed in the preparation of selective enzyme inhibito

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structure supports the creation of potent bioactive molecules, especially in the design of antidepressants and antipsychotics. The electron-withdrawing trifluoromethyl group enhances metabolic stability and improves blood-brain barrier penetration, making it valuable in medicinal chemistry. Also employed in the preparation of selective enzyme inhibitors due to its rigid heterocyclic framework and favorable binding properties.

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