1-(Aminomethyl)-2-oxabicyclo[2.1.1]hexane-4-carbonitrile

≥98%(GC)

Reagent Code: #130862
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CAS Number 2247107-84-0

science Other reagents with same CAS 2247107-84-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.17 g/mol
Formula C₇H₁₀N₂O
thermostat Physical Properties
Boiling Point 276.2±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.23±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of neuroactive compounds, particularly those targeting central nervous system disorders. Its rigid bicyclic structure enhances binding selectivity to certain neuronal receptors, making it valuable in developing drugs for epilepsy and neuropathic pain. Also explored in agrochemicals for designing bioactive molecules with improved metabolic stability. The presence of both nitrile and aminomethyl functional groups allows for further chemical modifications, enabling diverse derivatization in medicinal chemistry campaigns.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿19,110.00

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1-(Aminomethyl)-2-oxabicyclo[2.1.1]hexane-4-carbonitrile
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Used in pharmaceutical research as a key intermediate in the synthesis of neuroactive compounds, particularly those targeting central nervous system disorders. Its rigid bicyclic structure enhances binding selectivity to certain neuronal receptors, making it valuable in developing drugs for epilepsy and neuropathic pain. Also explored in agrochemicals for designing bioactive molecules with improved metabolic stability. The presence of both nitrile and aminomethyl functional groups allows for further chem

Used in pharmaceutical research as a key intermediate in the synthesis of neuroactive compounds, particularly those targeting central nervous system disorders. Its rigid bicyclic structure enhances binding selectivity to certain neuronal receptors, making it valuable in developing drugs for epilepsy and neuropathic pain. Also explored in agrochemicals for designing bioactive molecules with improved metabolic stability. The presence of both nitrile and aminomethyl functional groups allows for further chemical modifications, enabling diverse derivatization in medicinal chemistry campaigns.

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