(R)-2-chloro-5,6,7,8,9,10-hexahydrocyclohepta[b]indole-6-carboxamide

96%

Reagent Code: #232365
label
Alias Related 848193-72-6
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CAS Number 848193-73-7

science Other reagents with same CAS 848193-73-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.74 g/mol
Formula C₁₄H₁₅ClN₂O
inventory_2 Storage & Handling
Storage 2-8 °C, sealed, dry

description Product Description

Used in the synthesis of pharmaceutical agents targeting neurological disorders, particularly as an intermediate in developing serotonin receptor modulators. Its structural configuration supports high selectivity in binding, making it valuable in creating drugs for anxiety, depression, and migraine treatment. The compound’s chiral center enhances its biological activity, allowing lower therapeutic doses and reduced side effects. It is also explored in the development of anti-inflammatory agents due to its interaction with central nervous system pathways involved in pain modulation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿59,940.00
inventory 25mg
10-20 days ฿189,500.00
(R)-2-chloro-5,6,7,8,9,10-hexahydrocyclohepta[b]indole-6-carboxamide
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Used in the synthesis of pharmaceutical agents targeting neurological disorders, particularly as an intermediate in developing serotonin receptor modulators. Its structural configuration supports high selectivity in binding, making it valuable in creating drugs for anxiety, depression, and migraine treatment. The compound’s chiral center enhances its biological activity, allowing lower therapeutic doses and reduced side effects. It is also explored in the development of anti-inflammatory agents due to it

Used in the synthesis of pharmaceutical agents targeting neurological disorders, particularly as an intermediate in developing serotonin receptor modulators. Its structural configuration supports high selectivity in binding, making it valuable in creating drugs for anxiety, depression, and migraine treatment. The compound’s chiral center enhances its biological activity, allowing lower therapeutic doses and reduced side effects. It is also explored in the development of anti-inflammatory agents due to its interaction with central nervous system pathways involved in pain modulation.

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