6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazin-2-amine

95%

Reagent Code: #196507
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CAS Number 1779573-25-9

science Other reagents with same CAS 1779573-25-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.16 g/mol
Formula C₆H₉N₃O
inventory_2 Storage & Handling
Storage 2-8°C, preserved from light, dry sealed

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 modulators of neurotransmitter receptors, making it valuable in research for anxiolytic and anticonvulsant drugs. The amine functionality allows for easy derivatization, enabling rapid exploration of structure-activity relationships in drug discovery programs. It is also employed in the preparation of heterocyclic scaffolds for high-throughput screening in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿28,160.00
inventory 250mg
10-20 days ฿50,880.00

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6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazin-2-amine
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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 modulators of neurotransmitter receptors, making it valuable in research for anxiolytic and anticonvulsant drugs. The amine functionality allows for easy derivatization, enabling rapid exploration of structure-activity relationships in drug discovery programs. It is also employed in the preparation of heterocy

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 modulators of neurotransmitter receptors, making it valuable in research for anxiolytic and anticonvulsant drugs. The amine functionality allows for easy derivatization, enabling rapid exploration of structure-activity relationships in drug discovery programs. It is also employed in the preparation of heterocyclic scaffolds for high-throughput screening in medicinal chemistry.

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