(S)-3-(7-Bromo-1H-indol-3-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid

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Reagent Code: #232602
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CAS Number 612484-55-6

science Other reagents with same CAS 612484-55-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 383.24 g/mol
Formula C₁₆H₁₉BrN₂O₄
badge Registry Numbers
MDL Number MFCD09264334
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting neurological and psychiatric disorders. Its structure supports the construction of complex indole-based molecules, which are common in serotonin receptor modulators and kinase inhibitors. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step peptide-like syntheses. Commonly employed in research settings for designing novel therapeutics with improved selectivity and metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,120.00

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(S)-3-(7-Bromo-1H-indol-3-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting neurological and psychiatric disorders. Its structure supports the construction of complex indole-based molecules, which are common in serotonin receptor modulators and kinase inhibitors. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step peptide-like syntheses. Commonly employed in research settings for designing nov

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting neurological and psychiatric disorders. Its structure supports the construction of complex indole-based molecules, which are common in serotonin receptor modulators and kinase inhibitors. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step peptide-like syntheses. Commonly employed in research settings for designing novel therapeutics with improved selectivity and metabolic stability.

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