(S)-2-((tert-Butoxycarbonyl)amino)-3-(6-fluoro-1H-indol-3-yl)propanoic acid

95%

Reagent Code: #233428
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CAS Number 1234870-95-1

science Other reagents with same CAS 1234870-95-1

blur_circular Chemical Specifications

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Weight 322.33 g/mol
Formula C₁₆H₁₉FN₂O₄
badge Registry Numbers
MDL Number MFCD11656818
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor agonists and antagonists. Its indole structure with a fluorine substituent makes it valuable for creating biologically active molecules with enhanced metabolic stability and receptor selectivity. Commonly employed in peptide-based drug design and in the preparation of intermediates for central nervous system agents. The Boc-protected amine allows for controlled stepwise synthesis in solid-phase or solution-phase peptide coupling reactions.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿10,450.00
inventory 250mg
10-20 days ฿35,560.00

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(S)-2-((tert-Butoxycarbonyl)amino)-3-(6-fluoro-1H-indol-3-yl)propanoic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor agonists and antagonists. Its indole structure with a fluorine substituent makes it valuable for creating biologically active molecules with enhanced metabolic stability and receptor selectivity. Commonly employed in peptide-based drug design and in the preparation of intermediates for central nervous system agents. The Boc-protected amine allows for controlled stepwise synthesis in

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of serotonin receptor agonists and antagonists. Its indole structure with a fluorine substituent makes it valuable for creating biologically active molecules with enhanced metabolic stability and receptor selectivity. Commonly employed in peptide-based drug design and in the preparation of intermediates for central nervous system agents. The Boc-protected amine allows for controlled stepwise synthesis in solid-phase or solution-phase peptide coupling reactions.

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