5-Oxa-2-azaspiro[3.4]octan-7-onehydrochloride

95%

Reagent Code: #222462
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CAS Number 2306271-65-6

science Other reagents with same CAS 2306271-65-6

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Weight 163.6 g/mol
Formula C₆H₁₀ClNO₂
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Storage Room temperature

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its spirocyclic structure contributes to conformational rigidity, making it valuable in designing potent and selective drug candidates. Commonly employed in medicinal chemistry for optimizing metabolic stability and improving binding affinity in neuroactive drugs. Also explored in the synthesis of novel antibiotics and enzyme inhibitors due to its unique heterobicyclic framework.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,990.00
inventory 250mg
10-20 days ฿19,110.00
inventory 500mg
10-20 days ฿33,510.00
inventory 1g
10-20 days ฿58,640.00

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5-Oxa-2-azaspiro[3.4]octan-7-onehydrochloride
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its spirocyclic structure contributes to conformational rigidity, making it valuable in designing potent and selective drug candidates. Commonly employed in medicinal chemistry for optimizing metabolic stability and improving binding affinity in neuroactive drugs. Also explored in the synthesis of novel antibiotics and enzyme inhibitors

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Its spirocyclic structure contributes to conformational rigidity, making it valuable in designing potent and selective drug candidates. Commonly employed in medicinal chemistry for optimizing metabolic stability and improving binding affinity in neuroactive drugs. Also explored in the synthesis of novel antibiotics and enzyme inhibitors due to its unique heterobicyclic framework.

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