2-(Tert-Butoxycarbonyl)-5-Oxa-2-Azaspiro[3.4]Octane-7-Carboxylic Acid

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Reagent Code: #242325
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CAS Number 1251009-46-7

science Other reagents with same CAS 1251009-46-7

blur_circular Chemical Specifications

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Weight 257.28 g/mol
Formula C₁₂H₁₉NO₅
badge Registry Numbers
MDL Number MFCD14581235
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with spirocyclic frameworks. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like coupling reactions and heterocyclic chemistry. Commonly employed in medicinal chemistry for constructing structurally complex scaffolds, especially in drug discovery programs targeting central nervous system disorders and metabolic diseases. The Boc-protected amine allows for selective deprotection and further functionalization, enabling stepwise assembly of multi-component molecules. Its rigid spiro structure contributes to enhanced metabolic stability and improved pharmacokinetic profiles in lead compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,660.00
inventory 250mg
10-20 days ฿32,760.00
inventory 1g
10-20 days ฿65,520.00

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2-(Tert-Butoxycarbonyl)-5-Oxa-2-Azaspiro[3.4]Octane-7-Carboxylic Acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with spirocyclic frameworks. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like coupling reactions and heterocyclic chemistry. Commonly employed in medicinal chemistry for constructing structurally complex scaffolds, especially in drug discovery programs targeting central nervous system disorders and metabolic diseases. The Boc-protected amine
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with spirocyclic frameworks. Its protected amine and carboxylic acid functionalities make it valuable in peptide-like coupling reactions and heterocyclic chemistry. Commonly employed in medicinal chemistry for constructing structurally complex scaffolds, especially in drug discovery programs targeting central nervous system disorders and metabolic diseases. The Boc-protected amine allows for selective deprotection and further functionalization, enabling stepwise assembly of multi-component molecules. Its rigid spiro structure contributes to enhanced metabolic stability and improved pharmacokinetic profiles in lead compounds.
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