9-(tert-Butoxycarbonyl)-4-methyl-1-oxa-4,9-diazaspiro[5.5]undecane-2-carboxylic acid

95%

Reagent Code: #121036
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CAS Number 1824018-10-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.38 g/mol
Formula C₁₅H₂₆N₂O₅
badge Registry Numbers
MDL Number MFCD28119001
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the production of complex pharmaceutical compounds. Its unique structure, featuring a spirocyclic ring system and a protected amine group, makes it valuable for constructing molecules with specific biological activities. It is often employed in the synthesis of drugs targeting neurological disorders, as the spirocyclic framework can mimic certain natural substrates or receptors in the brain. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling further functionalization of the molecule during multi-step synthetic processes. Its application is also seen in the development of peptidomimetics, where it serves as a building block to mimic peptide structures, enhancing stability and bioavailability of potential drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿23,850.00
9-(tert-Butoxycarbonyl)-4-methyl-1-oxa-4,9-diazaspiro[5.5]undecane-2-carboxylic acid
This chemical is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the production of complex pharmaceutical compounds. Its unique structure, featuring a spirocyclic ring system and a protected amine group, makes it valuable for constructing molecules with specific biological activities. It is often employed in the synthesis of drugs targeting neurological disorders, as the spirocyclic framework can mimic certain natural substrates or receptors in the brain. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling further functionalization of the molecule during multi-step synthetic processes. Its application is also seen in the development of peptidomimetics, where it serves as a building block to mimic peptide structures, enhancing stability and bioavailability of potential drug candidates.
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