(Aminomethyl)cyclopropane hydrochloride

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Reagent Code: #137328
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CAS Number 7252-53-1

science Other reagents with same CAS 7252-53-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 107.58 g/mol
Formula C₄H₉N
badge Registry Numbers
MDL Number MFCD00012544
thermostat Physical Properties
Melting Point 200 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and antiviral drugs. Its rigid cyclopropane structure combined with the reactive aminomethyl group makes it valuable for constructing bioactive molecules with enhanced metabolic stability and target selectivity. It is also employed in the development of novel receptor agonists and antagonists, where the cyclopropane ring contributes to conformational restriction, improving potency and specificity. Additionally, it finds use in medicinal chemistry research for structure-activity relationship (SAR) studies due to its unique steric and electronic properties.

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inventory 1g
10-20 days ฿4,240.00

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(Aminomethyl)cyclopropane hydrochloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and antiviral drugs. Its rigid cyclopropane structure combined with the reactive aminomethyl group makes it valuable for constructing bioactive molecules with enhanced metabolic stability and target selectivity. It is also employed in the development of novel receptor agonists and antagonists, where the cyclopropane ring contributes to conformational restrictio

Used primarily as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and antiviral drugs. Its rigid cyclopropane structure combined with the reactive aminomethyl group makes it valuable for constructing bioactive molecules with enhanced metabolic stability and target selectivity. It is also employed in the development of novel receptor agonists and antagonists, where the cyclopropane ring contributes to conformational restriction, improving potency and specificity. Additionally, it finds use in medicinal chemistry research for structure-activity relationship (SAR) studies due to its unique steric and electronic properties.

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