2-Phenyl-3-(piperidin-4-yl)-1H-indole

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Reagent Code: #227442
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CAS Number 221109-26-8

science Other reagents with same CAS 221109-26-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.391 g/mol
Formula C₁₉H₂₂N₂
badge Registry Numbers
MDL Number MFCD03426314
thermostat Physical Properties
Boiling Point 484 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a key intermediate for developing central nervous system (CNS) active compounds. Shows potential in the synthesis of serotonin receptor modulators, particularly targeting 5-HT3 and 5-HT6 receptors, which are involved in mood regulation, cognition, and nausea control. Investigated for use in treatments of psychiatric disorders such as depression, anxiety, and schizophrenia. Also explored for analgesic applications due to structural affinity with known pain-modulating agents. Its piperidine-indole framework supports blood-brain barrier penetration, making it suitable for neuropharmacological drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿47,910.00

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2-Phenyl-3-(piperidin-4-yl)-1H-indole
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Used in pharmaceutical research as a key intermediate for developing central nervous system (CNS) active compounds. Shows potential in the synthesis of serotonin receptor modulators, particularly targeting 5-HT3 and 5-HT6 receptors, which are involved in mood regulation, cognition, and nausea control. Investigated for use in treatments of psychiatric disorders such as depression, anxiety, and schizophrenia. Also explored for analgesic applications due to structural affinity with known pain-modulating age

Used in pharmaceutical research as a key intermediate for developing central nervous system (CNS) active compounds. Shows potential in the synthesis of serotonin receptor modulators, particularly targeting 5-HT3 and 5-HT6 receptors, which are involved in mood regulation, cognition, and nausea control. Investigated for use in treatments of psychiatric disorders such as depression, anxiety, and schizophrenia. Also explored for analgesic applications due to structural affinity with known pain-modulating agents. Its piperidine-indole framework supports blood-brain barrier penetration, making it suitable for neuropharmacological drug design.

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