(3-endo)-tert-Butyl 3-(hydroxymethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate

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Reagent Code: #141159
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CAS Number 273376-39-9

science Other reagents with same CAS 273376-39-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.33 g/mol
Formula C₁₃H₂₃NO₃
badge Registry Numbers
MDL Number MFCD29037442
thermostat Physical Properties
Boiling Point 342.5±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.098±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of a hydroxymethyl group and a protected amine, allowing for selective modifications. Commonly employed in the preparation of tropane-based compounds, which are relevant in the design of receptor antagonists and enzyme inhibitors. Also utilized in medicinal chemistry for building blocks in the discovery of treatments for neurological disorders.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,050.00
inventory 500mg
10-20 days ฿34,750.00
inventory 1g
10-20 days ฿52,040.00

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(3-endo)-tert-Butyl 3-(hydroxymethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of a hydroxymethyl group and a protected amine, allowing for selective modifications. Commonly employed in the preparation of tropane-based compounds, which are relevant in the design of receptor antagonists and enzyme inhibitors. Also utilized in medicinal chemistry for building blocks in the discovery o
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of a hydroxymethyl group and a protected amine, allowing for selective modifications. Commonly employed in the preparation of tropane-based compounds, which are relevant in the design of receptor antagonists and enzyme inhibitors. Also utilized in medicinal chemistry for building blocks in the discovery of treatments for neurological disorders.
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