7-(tert-Butoxycarbonyl)-2-oxa-7-azaspiro-[4.5]decane-3-carboxylic acid

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Reagent Code: #86857
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CAS Number 1160246-92-3

science Other reagents with same CAS 1160246-92-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.34 g/mol
Formula C₁₄H₂₃NO₅
badge Registry Numbers
MDL Number MFCD12198530
inventory_2 Storage & Handling
Storage 2-8°C, dry, airtight

description Product Description

This chemical is primarily used in organic synthesis, particularly in the development of complex molecules. It serves as a key intermediate in the preparation of pharmaceuticals, especially those targeting neurological and psychiatric disorders. Its structure, featuring a spirocyclic system, makes it valuable for constructing rigid frameworks in drug molecules, enhancing stability and bioavailability. Additionally, it is employed in peptide chemistry, where it acts as a protecting group for amines during synthesis, ensuring selective reactions. Its tert-butoxycarbonyl (Boc) group is easily removable under mild conditions, making it a versatile tool in multi-step synthetic processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,920.00
inventory 250mg
10-20 days ฿25,650.00

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7-(tert-Butoxycarbonyl)-2-oxa-7-azaspiro-[4.5]decane-3-carboxylic acid
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This chemical is primarily used in organic synthesis, particularly in the development of complex molecules. It serves as a key intermediate in the preparation of pharmaceuticals, especially those targeting neurological and psychiatric disorders. Its structure, featuring a spirocyclic system, makes it valuable for constructing rigid frameworks in drug molecules, enhancing stability and bioavailability. Additionally, it is employed in peptide chemistry, where it acts as a protecting group for amines during

This chemical is primarily used in organic synthesis, particularly in the development of complex molecules. It serves as a key intermediate in the preparation of pharmaceuticals, especially those targeting neurological and psychiatric disorders. Its structure, featuring a spirocyclic system, makes it valuable for constructing rigid frameworks in drug molecules, enhancing stability and bioavailability. Additionally, it is employed in peptide chemistry, where it acts as a protecting group for amines during synthesis, ensuring selective reactions. Its tert-butoxycarbonyl (Boc) group is easily removable under mild conditions, making it a versatile tool in multi-step synthetic processes.

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