6-Oxa-2-azaspiro[3.5]nonane hydrochloride

95%

Reagent Code: #222128
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CAS Number 1359656-29-3

science Other reagents with same CAS 1359656-29-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.65 g/mol
Formula C₇H₁₄ClNO
badge Registry Numbers
MDL Number MFCD21364492
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and cognitive enhancers. Its spirocyclic structure contributes to conformational rigidity, making it valuable in drug design for improving selectivity and metabolic stability. Commonly employed in the preparation of nootropic and neuroprotective compounds. Also utilized in research settings for exploring structure-activity relationships in heterocyclic amines.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,000.00
inventory 250mg
10-20 days ฿12,800.00
inventory 1g
10-20 days ฿33,600.00
inventory 5g
10-20 days ฿131,200.00

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6-Oxa-2-azaspiro[3.5]nonane hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and cognitive enhancers. Its spirocyclic structure contributes to conformational rigidity, making it valuable in drug design for improving selectivity and metabolic stability. Commonly employed in the preparation of nootropic and neuroprotective compounds. Also utilized in research settings for exploring structure-activity relationships in heterocyclic amines.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and cognitive enhancers. Its spirocyclic structure contributes to conformational rigidity, making it valuable in drug design for improving selectivity and metabolic stability. Commonly employed in the preparation of nootropic and neuroprotective compounds. Also utilized in research settings for exploring structure-activity relationships in heterocyclic amines.

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