8-Amino-4H-1,4-Benzoxazin-3-One

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Reagent Code: #138735
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CAS Number 1042973-67-0

science Other reagents with same CAS 1042973-67-0

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Weight 198.61 g/mol
Formula C₈H₇ClN₂O₂
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. It serves as a building block for heterocyclic structures found in anxiolytic and anticonvulsant drugs. Its scaffold is valuable in medicinal chemistry for designing molecules with improved bioavailability and receptor selectivity. Also employed in research settings to explore new bioactive molecules and in the preparation of fluorescent probes due to its favorable ring structure and functional group reactivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,970.00
inventory 250mg
10-20 days ฿6,850.00
inventory 1g
10-20 days ฿11,670.00

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8-Amino-4H-1,4-Benzoxazin-3-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. It serves as a building block for heterocyclic structures found in anxiolytic and anticonvulsant drugs. Its scaffold is valuable in medicinal chemistry for designing molecules with improved bioavailability and receptor selectivity. Also employed in research settings to explore new bioactive molecules and in the preparation of fluorescent probes due to its

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. It serves as a building block for heterocyclic structures found in anxiolytic and anticonvulsant drugs. Its scaffold is valuable in medicinal chemistry for designing molecules with improved bioavailability and receptor selectivity. Also employed in research settings to explore new bioactive molecules and in the preparation of fluorescent probes due to its favorable ring structure and functional group reactivity.

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