Methyl 3-azabicyclo[3.2.1]octane-8-carboxylate hydrochloride

97%

Reagent Code: #128868
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CAS Number 1403766-94-8

science Other reagents with same CAS 1403766-94-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.68 g/mol
Formula C₉H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD23105857
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in pharmaceutical synthesis as a key intermediate for developing bioactive molecules, particularly in the production of centrally acting agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for enhancing selectivity and stability in drug candidates. Commonly employed in the development of neurological and psychiatric disorder treatments due to its structural similarity to known neuroactive scaffolds. Also utilized in the design of receptor ligands targeting nicotinic acetylcholine receptors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,820.00
inventory 250mg
10-20 days ฿15,690.00
inventory 1g
10-20 days ฿39,120.00
Methyl 3-azabicyclo[3.2.1]octane-8-carboxylate hydrochloride
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Used in pharmaceutical synthesis as a key intermediate for developing bioactive molecules, particularly in the production of centrally acting agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for enhancing selectivity and stability in drug candidates. Commonly employed in the development of neurological and psychiatric disorder treatments due to its structural similarity to known neuroactive scaffolds. Also utilized in the design of receptor ligands targeting nicotinic acetylchol
Used in pharmaceutical synthesis as a key intermediate for developing bioactive molecules, particularly in the production of centrally acting agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for enhancing selectivity and stability in drug candidates. Commonly employed in the development of neurological and psychiatric disorder treatments due to its structural similarity to known neuroactive scaffolds. Also utilized in the design of receptor ligands targeting nicotinic acetylcholine receptors.
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