1-Boc-4-oxo-1-azaspiro[5.5]undecane

95%

Reagent Code: #46907
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CAS Number 778647-35-1

science Other reagents with same CAS 778647-35-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.3600 g/mol
Formula C₁₅H₂₅NO₃
badge Registry Numbers
MDL Number MFCD09283648
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a key building block in the development of compounds with potential therapeutic applications, such as inhibitors or modulators of biological targets. The Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. Its spirocyclic structure contributes to the rigidity and stability of the resulting compounds, making it valuable in drug discovery and medicinal chemistry. Additionally, it can be employed in the synthesis of natural products or bioactive molecules with spirocyclic frameworks.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,067.00

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1-Boc-4-oxo-1-azaspiro[5.5]undecane
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This chemical is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a key building block in the development of compounds with potential therapeutic applications, such as inhibitors or modulators of biological targets. The Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. Its spirocyclic structure cont

This chemical is primarily used in organic synthesis as a versatile intermediate for the preparation of more complex molecules, particularly in pharmaceutical research. It serves as a key building block in the development of compounds with potential therapeutic applications, such as inhibitors or modulators of biological targets. The Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. Its spirocyclic structure contributes to the rigidity and stability of the resulting compounds, making it valuable in drug discovery and medicinal chemistry. Additionally, it can be employed in the synthesis of natural products or bioactive molecules with spirocyclic frameworks.

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