3-(Piperidin-4-ylmethyl)-1H-indole

≥95%

Reagent Code: #226242
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CAS Number 3515-49-9

science Other reagents with same CAS 3515-49-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.31 g/mol
Formula C₁₄H₁₈N₂
badge Registry Numbers
MDL Number MFCD01718591
thermostat Physical Properties
Boiling Point 401.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of serotonin receptor modulators. Shows potential in developing treatments for neurological disorders such as depression, anxiety, and schizophrenia. Also explored for its role in creating selective agonists and antagonists targeting 5-HT receptors. Its structure supports blood-brain barrier penetration, making it valuable in central nervous system drug design. Investigated in the development of anti-migraine agents and cognitive enhancers. Commonly modified to improve binding affinity and metabolic stability in drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,920.00
inventory 100mg
10-20 days ฿9,460.00
inventory 250mg
10-20 days ฿15,960.00
inventory 1g
10-20 days ฿43,420.00
3-(Piperidin-4-ylmethyl)-1H-indole
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Used in pharmaceutical research as a key intermediate in the synthesis of serotonin receptor modulators. Shows potential in developing treatments for neurological disorders such as depression, anxiety, and schizophrenia. Also explored for its role in creating selective agonists and antagonists targeting 5-HT receptors. Its structure supports blood-brain barrier penetration, making it valuable in central nervous system drug design. Investigated in the development of anti-migraine agents and cognitive enha

Used in pharmaceutical research as a key intermediate in the synthesis of serotonin receptor modulators. Shows potential in developing treatments for neurological disorders such as depression, anxiety, and schizophrenia. Also explored for its role in creating selective agonists and antagonists targeting 5-HT receptors. Its structure supports blood-brain barrier penetration, making it valuable in central nervous system drug design. Investigated in the development of anti-migraine agents and cognitive enhancers. Commonly modified to improve binding affinity and metabolic stability in drug candidates.

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