tert-butyl 4-(1H-indol-3-yl)piperidine-1-carboxylate

98%

Reagent Code: #83770
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CAS Number 155302-28-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.40 g/mol
Formula C₁₈H₂₄N₂O₂
badge Registry Numbers
MDL Number MFCD11840339
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and psychiatric disorders. Its structure, featuring an indole moiety, makes it valuable for designing molecules that interact with serotonin receptors, which are crucial in treating conditions like depression, anxiety, and migraines. Additionally, it is employed in the creation of pharmaceutical agents that modulate other central nervous system pathways, contributing to the development of novel therapies. Its piperidine and tert-butyl carboxylate groups further enhance its utility in optimizing drug-like properties, such as stability and bioavailability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,004.00
inventory 250mg
10-20 days ฿8,505.00
inventory 1g
10-20 days ฿26,730.00
tert-butyl 4-(1H-indol-3-yl)piperidine-1-carboxylate
This chemical is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and psychiatric disorders. Its structure, featuring an indole moiety, makes it valuable for designing molecules that interact with serotonin receptors, which are crucial in treating conditions like depression, anxiety, and migraines. Additionally, it is employed in the creation of pharmaceutical agents that modulate other central nervous system pathways, contributing to the development of novel therapies. Its piperidine and tert-butyl carboxylate groups further enhance its utility in optimizing drug-like properties, such as stability and bioavailability.
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