(4AS,8aS,9S)-3-(benzyloxy)-4a-((tert-butyldimethylsilyl)oxy)-9-(dimethylamino)-8a,9-dihydronaphtho[2,3-d]isoxazole-4,5(4aH,8H)-dione

97%

Reagent Code: #36956
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CAS Number 852821-06-8

science Other reagents with same CAS 852821-06-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 482.64 g/mol
Formula C₂₆H₃₄N₂O₅Si
badge Registry Numbers
MDL Number MFCD28023585
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the development of complex molecules, particularly in pharmaceutical research. Its structural features, including the benzyloxy and tert-butyldimethylsilyloxy groups, make it valuable for selective protection and deprotection strategies during multi-step synthetic processes. The dimethylamino group enhances its reactivity, enabling its use in the construction of nitrogen-containing heterocycles, which are common in bioactive compounds. Researchers often employ it in the synthesis of potential drug candidates targeting neurological or oncological disorders, leveraging its unique scaffold to explore structure-activity relationships. Additionally, its stability and functional groups allow for further modifications, making it a versatile tool in medicinal chemistry.

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Test Parameter Specification
Appearance White to light-yellow powder or crystals
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,654.00
inventory 1g
10-20 days ฿14,652.00
inventory 250mg
10-20 days ฿5,859.00

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(4AS,8aS,9S)-3-(benzyloxy)-4a-((tert-butyldimethylsilyl)oxy)-9-(dimethylamino)-8a,9-dihydronaphtho[2,3-d]isoxazole-4,5(4aH,8H)-dione
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This compound is primarily utilized in organic synthesis as an intermediate for the development of complex molecules, particularly in pharmaceutical research. Its structural features, including the benzyloxy and tert-butyldimethylsilyloxy groups, make it valuable for selective protection and deprotection strategies during multi-step synthetic processes. The dimethylamino group enhances its reactivity, enabling its use in the construction of nitrogen-containing heterocycles, which are common in bioactive

This compound is primarily utilized in organic synthesis as an intermediate for the development of complex molecules, particularly in pharmaceutical research. Its structural features, including the benzyloxy and tert-butyldimethylsilyloxy groups, make it valuable for selective protection and deprotection strategies during multi-step synthetic processes. The dimethylamino group enhances its reactivity, enabling its use in the construction of nitrogen-containing heterocycles, which are common in bioactive compounds. Researchers often employ it in the synthesis of potential drug candidates targeting neurological or oncological disorders, leveraging its unique scaffold to explore structure-activity relationships. Additionally, its stability and functional groups allow for further modifications, making it a versatile tool in medicinal chemistry.

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