4-cyclopropylcyclohexan-1-amine, Mixture of diastereomers

≥95%

Reagent Code: #203775
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CAS Number 1449582-41-5

science Other reagents with same CAS 1449582-41-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.238 g/mol
Formula C₉H₁₇N
badge Registry Numbers
MDL Number MFCD26031238
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. Its rigid cyclohexyl-cyclopropyl scaffold enhances binding selectivity to certain neuronal receptors, making it valuable in the design of neuroactive drugs. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical complexity. Also utilized in the preparation of protease inhibitors and receptor modulators where conformational restraint improves metabolic stability and potency.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿24,000.00
inventory 250mg
10-20 days ฿44,800.00
inventory 1g
10-20 days ฿128,720.00

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4-cyclopropylcyclohexan-1-amine, Mixture of diastereomers
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. Its rigid cyclohexyl-cyclopropyl scaffold enhances binding selectivity to certain neuronal receptors, making it valuable in the design of neuroactive drugs. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical complexity. Also utilized in the preparation of protease inhibitors and receptor modulator

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. Its rigid cyclohexyl-cyclopropyl scaffold enhances binding selectivity to certain neuronal receptors, making it valuable in the design of neuroactive drugs. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical complexity. Also utilized in the preparation of protease inhibitors and receptor modulators where conformational restraint improves metabolic stability and potency.

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