tert-Butyl endo-3-amino-8-azabicyclo[3.2.1]octane-8-carboxylate

96%

Reagent Code: #145362
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CAS Number 207405-68-3

science Other reagents with same CAS 207405-68-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.32 g/mol
Formula C₁₂H₂₂N₂O₂
thermostat Physical Properties
Boiling Point 313.2°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as dopamine and serotonin modulators. Its rigid bicyclic structure and protected amine functionality make it valuable in medicinal chemistry for constructing bioactive molecules with enhanced selectivity and metabolic stability. Commonly employed in the preparation of neuroactive drugs, including antidepressants and antipsychotics, where the scaffold contributes to blood-brain barrier penetration and receptor binding affinity. Also utilized in asymmetric synthesis and as a chiral building block in the design of enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿690.00
inventory 1g
10-20 days ฿1,520.00
inventory 5g
10-20 days ฿5,200.00
inventory 25g
10-20 days ฿21,500.00
inventory 10g
10-20 days ฿9,500.00

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tert-Butyl endo-3-amino-8-azabicyclo[3.2.1]octane-8-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as dopamine and serotonin modulators. Its rigid bicyclic structure and protected amine functionality make it valuable in medicinal chemistry for constructing bioactive molecules with enhanced selectivity and metabolic stability. Commonly employed in the preparation of neuroactive drugs, including antidepressants and antipsychotics, where the scaffold contributes to blood-brain b

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of centrally acting agents such as dopamine and serotonin modulators. Its rigid bicyclic structure and protected amine functionality make it valuable in medicinal chemistry for constructing bioactive molecules with enhanced selectivity and metabolic stability. Commonly employed in the preparation of neuroactive drugs, including antidepressants and antipsychotics, where the scaffold contributes to blood-brain barrier penetration and receptor binding affinity. Also utilized in asymmetric synthesis and as a chiral building block in the design of enzyme inhibitors.

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