8,8-Dimethoxy-3-azabicyclo[3.2.1]octane

97%

Reagent Code: #178440
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CAS Number 1822844-21-2

science Other reagents with same CAS 1822844-21-2

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for designing compounds with specific stereochemistry and improved binding affinity. Commonly employed in the preparation of dopamine and serotonin receptor ligands. Also utilized in the creation of novel psychoactive substances for research purposes. Its methoxy groups allow further functionalization, enabling diverse derivatization for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,290.00
inventory 100mg
10-20 days ฿18,560.00

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8,8-Dimethoxy-3-azabicyclo[3.2.1]octane
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for designing compounds with specific stereochemistry and improved binding affinity. Commonly employed in the preparation of dopamine and serotonin receptor ligands. Also utilized in the creation of novel psychoactive substances for research purposes. Its methoxy groups allow further functionalization, enabling di

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents. Its rigid bicyclic structure makes it valuable in medicinal chemistry for designing compounds with specific stereochemistry and improved binding affinity. Commonly employed in the preparation of dopamine and serotonin receptor ligands. Also utilized in the creation of novel psychoactive substances for research purposes. Its methoxy groups allow further functionalization, enabling diverse derivatization for structure-activity relationship studies.

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