1-(Piperidin-4-yl)-1H-indole

98%

Reagent Code: #225429
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CAS Number 118511-81-2

science Other reagents with same CAS 118511-81-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.28 g/mol
Formula C₁₃H₁₆N₂
badge Registry Numbers
MDL Number MFCD07364487
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in pharmaceutical research as a key intermediate in the synthesis of serotonin receptor modulators. Its structure supports the development of compounds targeting neurological disorders such as depression, anxiety, and schizophrenia. The molecule’s indole and piperidine moieties enable strong binding affinity to 5-HT receptors, making it valuable in creating selective and potent drug candidates. Also explored in the design of novel analgesics and cognitive enhancers due to its ability to cross the blood-brain barrier effectively.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,190.00
inventory 100mg
10-20 days ฿5,310.00

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1-(Piperidin-4-yl)-1H-indole
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Used primarily in pharmaceutical research as a key intermediate in the synthesis of serotonin receptor modulators. Its structure supports the development of compounds targeting neurological disorders such as depression, anxiety, and schizophrenia. The molecule’s indole and piperidine moieties enable strong binding affinity to 5-HT receptors, making it valuable in creating selective and potent drug candidates. Also explored in the design of novel analgesics and cognitive enhancers due to its ability to cr

Used primarily in pharmaceutical research as a key intermediate in the synthesis of serotonin receptor modulators. Its structure supports the development of compounds targeting neurological disorders such as depression, anxiety, and schizophrenia. The molecule’s indole and piperidine moieties enable strong binding affinity to 5-HT receptors, making it valuable in creating selective and potent drug candidates. Also explored in the design of novel analgesics and cognitive enhancers due to its ability to cross the blood-brain barrier effectively.

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