2-(5-((Pyrrolidin-1-ylsulfonyl)methyl)-1H-indol-3-yl)ethanamine hemifumarate

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Reagent Code: #223251
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CAS Number 1246860-65-0

science Other reagents with same CAS 1246860-65-0

blur_circular Chemical Specifications

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Weight 730.9 g/mol
Formula C₃₄H₄₆N₆O₈S₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in pharmaceutical research as a key intermediate in the synthesis of selective serotonin reuptake inhibitors (SSRIs). Its structure supports the development of compounds targeting central nervous system disorders, particularly depression and anxiety. The molecule’s indole core and amine functionality enhance binding affinity to serotonin transporters, making it valuable in optimizing drug efficacy and metabolic stability. It is also explored in the design of novel neuroactive agents due to its favorable solubility and salt-forming properties when combined with fumaric acid.

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Size Availability Unit Price Quantity
inventory 15mg
10-20 days ฿113,800.00

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2-(5-((Pyrrolidin-1-ylsulfonyl)methyl)-1H-indol-3-yl)ethanamine hemifumarate
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Used primarily in pharmaceutical research as a key intermediate in the synthesis of selective serotonin reuptake inhibitors (SSRIs). Its structure supports the development of compounds targeting central nervous system disorders, particularly depression and anxiety. The molecule’s indole core and amine functionality enhance binding affinity to serotonin transporters, making it valuable in optimizing drug efficacy and metabolic stability. It is also explored in the design of novel neuroactive agents due to it
Used primarily in pharmaceutical research as a key intermediate in the synthesis of selective serotonin reuptake inhibitors (SSRIs). Its structure supports the development of compounds targeting central nervous system disorders, particularly depression and anxiety. The molecule’s indole core and amine functionality enhance binding affinity to serotonin transporters, making it valuable in optimizing drug efficacy and metabolic stability. It is also explored in the design of novel neuroactive agents due to its favorable solubility and salt-forming properties when combined with fumaric acid.
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