(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromo-1H-indol-3-yl)propanoic acid

95%

Reagent Code: #236180
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CAS Number 460751-66-0

science Other reagents with same CAS 460751-66-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 505.36 g/mol
Formula C₂₆H₂₁BrN₂O₄
badge Registry Numbers
MDL Number MFCD28166519
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for incorporating tryptophan analogs into peptide chains. The Fmoc group allows for mild base-labile protection, enabling stepwise assembly of peptides in solid-phase synthesis. The brominated indole moiety enhances reactivity in cross-coupling reactions, making it valuable for generating modified peptides with tailored properties, such as improved binding affinity or metabolic stability. It is also employed in the development of bioactive peptides and pharmaceutical intermediates where precise structural control is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,460.00
inventory 500mg
10-20 days ฿10,230.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromo-1H-indol-3-yl)propanoic acid
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Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for incorporating tryptophan analogs into peptide chains. The Fmoc group allows for mild base-labile protection, enabling stepwise assembly of peptides in solid-phase synthesis. The brominated indole moiety enhances reactivity in cross-coupling reactions, making it valuable for generating modified peptides with tailored properties, such as improved binding affinity or metabolic stability. It is also employed in the development of bioactive peptides and pharmaceutical intermediates where precise structural control is required.
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