3-Oxa-8-Azaspiro[3.5]Nonane-8-Carboxylic Acid Tert-Butyl Ester

98%

Reagent Code: #222341
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CAS Number 1272412-68-6

science Other reagents with same CAS 1272412-68-6

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Weight 227.3 g/mol
Formula C₁₂H₂₁NO₃
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Storage Room temperature

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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its spirocyclic structure and embedded nitrogen make it valuable in medicinal chemistry for constructing bioactive molecules with improved metabolic stability and binding affinity. Commonly employed in the preparation of selective enzyme inhibitors and receptor modulators, especially in research targeting neurological disorders. The tert-butyl ester group allows for easy protection during multi-step syntheses, enabling selective deprotection and further functionalization in drug design.

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inventory 100mg
10-20 days ฿21,040.00

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3-Oxa-8-Azaspiro[3.5]Nonane-8-Carboxylic Acid Tert-Butyl Ester
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its spirocyclic structure and embedded nitrogen make it valuable in medicinal chemistry for constructing bioactive molecules with improved metabolic stability and binding affinity. Commonly employed in the preparation of selective enzyme inhibitors and receptor modulators, especially in research targeting neurological disorders. The tert-butyl ester group allows for easy

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its spirocyclic structure and embedded nitrogen make it valuable in medicinal chemistry for constructing bioactive molecules with improved metabolic stability and binding affinity. Commonly employed in the preparation of selective enzyme inhibitors and receptor modulators, especially in research targeting neurological disorders. The tert-butyl ester group allows for easy protection during multi-step syntheses, enabling selective deprotection and further functionalization in drug design.

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