2-(2H-Benzo[b][1,4]oxazin-4(3H)-yl)-N-benzyl-5,6,7,8-tetrahydroquinazolin-4-amine

99%

Reagent Code: #101490
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CAS Number 1346528-06-0

science Other reagents with same CAS 1346528-06-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.463 g/mol
Formula C₂₃H₂₄N₄O
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate or active ingredient in the synthesis of potential therapeutic agents. Its structure is particularly valuable in the design of molecules targeting neurological disorders, as it exhibits properties that may interact with specific receptors in the brain. Additionally, it is explored for its potential anti-inflammatory and analgesic effects, making it a candidate for the development of pain management drugs. Researchers also investigate its role in modulating enzyme activity, which could lead to applications in treating metabolic or immune-related conditions. Its versatility in chemical modifications allows for the creation of derivatives with optimized pharmacological profiles.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿11,500.00
inventory 1mg
10-20 days ฿2,550.00

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2-(2H-Benzo[b][1,4]oxazin-4(3H)-yl)-N-benzyl-5,6,7,8-tetrahydroquinazolin-4-amine
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This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate or active ingredient in the synthesis of potential therapeutic agents. Its structure is particularly valuable in the design of molecules targeting neurological disorders, as it exhibits properties that may interact with specific receptors in the brain. Additionally, it is explored for its potential anti-inflammatory and analgesic effects, making it a candidate for the development of pain management drugs. Researchers also investigate its role in modulating enzyme activity, which could lead to applications in treating metabolic or immune-related conditions. Its versatility in chemical modifications allows for the creation of derivatives with optimized pharmacological profiles.
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