2-(N-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethyl)methylsulfonamido)acetic acid

98%

Reagent Code: #219004
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CAS Number 1335206-40-0

science Other reagents with same CAS 1335206-40-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 418.46 g/mol
Formula C₂₀H₂₂N₂O₆S
badge Registry Numbers
MDL Number MFCD26959160
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Widely used in peptide synthesis, this compound serves as a key reagent for introducing sulfonamide functionality while maintaining compatibility with Fmoc-based solid-phase strategies. Its primary application lies in the preparation of modified peptides and peptidomimetics, where the sulfonamide group enhances metabolic stability and influences conformation. The Fmoc-protected amine allows for controlled, stepwise assembly of peptide chains on solid support, making it valuable in medicinal chemistry for developing protease inhibitors and bioactive molecules. Additionally, it is employed in the synthesis of labeled peptides and conjugates for biochemical assays and imaging studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,850.00
inventory 250mg
10-20 days ฿5,070.00
inventory 1g
10-20 days ฿13,740.00
2-(N-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethyl)methylsulfonamido)acetic acid
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Widely used in peptide synthesis, this compound serves as a key reagent for introducing sulfonamide functionality while maintaining compatibility with Fmoc-based solid-phase strategies. Its primary application lies in the preparation of modified peptides and peptidomimetics, where the sulfonamide group enhances metabolic stability and influences conformation. The Fmoc-protected amine allows for controlled, stepwise assembly of peptide chains on solid support, making it valuable in medicinal chemistry for de
Widely used in peptide synthesis, this compound serves as a key reagent for introducing sulfonamide functionality while maintaining compatibility with Fmoc-based solid-phase strategies. Its primary application lies in the preparation of modified peptides and peptidomimetics, where the sulfonamide group enhances metabolic stability and influences conformation. The Fmoc-protected amine allows for controlled, stepwise assembly of peptide chains on solid support, making it valuable in medicinal chemistry for developing protease inhibitors and bioactive molecules. Additionally, it is employed in the synthesis of labeled peptides and conjugates for biochemical assays and imaging studies.
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