4-(3-Hydroxy-8-Azabicyclo[3.2.1]Oct-8-Yl)Naphthalene-1-Carbonitrile

99%

Reagent Code: #198518
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CAS Number 870888-46-3

science Other reagents with same CAS 870888-46-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.36 g/mol
Formula C₁₈H₁₈N₂O
badge Registry Numbers
MDL Number MFCD24386408
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of selective dopamine reuptake inhibitors. It plays a role in developing compounds targeting central nervous system disorders, particularly for potential use in treating attention deficit hyperactivity disorder (ADHD) and depression. Its structure allows for strong binding affinity to dopamine transporters, making it valuable in optimizing neuroactive drug candidates. Also investigated for use in positron emission tomography (PET) tracer development due to its ability to cross the blood-brain barrier and interact with specific neural targets.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿6,900.00
inventory 25mg
10-20 days ฿26,780.00
inventory 100mg
10-20 days ฿80,110.00

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4-(3-Hydroxy-8-Azabicyclo[3.2.1]Oct-8-Yl)Naphthalene-1-Carbonitrile
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Used in pharmaceutical research as a key intermediate in the synthesis of selective dopamine reuptake inhibitors. It plays a role in developing compounds targeting central nervous system disorders, particularly for potential use in treating attention deficit hyperactivity disorder (ADHD) and depression. Its structure allows for strong binding affinity to dopamine transporters, making it valuable in optimizing neuroactive drug candidates. Also investigated for use in positron emission tomography (PET) tra

Used in pharmaceutical research as a key intermediate in the synthesis of selective dopamine reuptake inhibitors. It plays a role in developing compounds targeting central nervous system disorders, particularly for potential use in treating attention deficit hyperactivity disorder (ADHD) and depression. Its structure allows for strong binding affinity to dopamine transporters, making it valuable in optimizing neuroactive drug candidates. Also investigated for use in positron emission tomography (PET) tracer development due to its ability to cross the blood-brain barrier and interact with specific neural targets.

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