(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-sulfophenyl)propanoic acid

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Reagent Code: #236624
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CAS Number 138472-22-7

science Other reagents with same CAS 138472-22-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 467.49 g/mol
Formula C₂₄H₂₁NO₇S
badge Registry Numbers
MDL Number MFCD01632249
inventory_2 Storage & Handling
Density 1.433±0.06 g/cm3(Predicted)
Storage Room temperature, sealed

description Product Description

Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for introducing tyrosine-like structures with enhanced solubility. The sulfonate group improves water solubility, making it valuable in solution-phase peptide coupling where polar intermediates are needed. It is especially useful in solid-phase synthesis when working with Fmoc-strategy, allowing mild deprotection conditions while maintaining side-chain protection. Its fluorescent properties, inherited from the fluorenyl group, enable detection during chromatography or purification steps. Commonly applied in the preparation of bioactive peptides, protein mimetics, and labeled peptides for biochemical assays.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,670.00
inventory 250mg
10-20 days ฿13,380.00
inventory 1g
10-20 days ฿39,940.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-sulfophenyl)propanoic acid
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Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for introducing tyrosine-like structures with enhanced solubility. The sulfonate group improves water solubility, making it valuable in solution-phase peptide coupling where polar intermediates are needed. It is especially useful in solid-phase synthesis when working with Fmoc-strategy, allowing mild deprotection conditions while maintaining side-chain protection. Its fluorescent properties, inherite

Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, specifically for introducing tyrosine-like structures with enhanced solubility. The sulfonate group improves water solubility, making it valuable in solution-phase peptide coupling where polar intermediates are needed. It is especially useful in solid-phase synthesis when working with Fmoc-strategy, allowing mild deprotection conditions while maintaining side-chain protection. Its fluorescent properties, inherited from the fluorenyl group, enable detection during chromatography or purification steps. Commonly applied in the preparation of bioactive peptides, protein mimetics, and labeled peptides for biochemical assays.

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