(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4,4-difluorobutanoic acid

96%

Reagent Code: #236968
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CAS Number 467442-21-3

science Other reagents with same CAS 467442-21-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 361.34 g/mol
Formula C₁₉H₁₇F₂NO₄
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Widely used in peptide synthesis, this compound serves as a protected chiral amino acid building block. Its main application lies in the preparation of modified peptides where enhanced metabolic stability and conformational control are required. The difluorinated side chain influences peptide backbone geometry and improves bioavailability, making it valuable in the development of pharmaceutical agents. The Fmoc group allows for mild, base-labile protection during solid-phase synthesis, enabling stepwise assembly of complex peptides. It is particularly useful in research settings focused on structure-activity relationship studies of bioactive peptides.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,250.00
inventory 250mg
10-20 days ฿6,360.00
inventory 1g
10-20 days ฿25,280.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4,4-difluorobutanoic acid
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Widely used in peptide synthesis, this compound serves as a protected chiral amino acid building block. Its main application lies in the preparation of modified peptides where enhanced metabolic stability and conformational control are required. The difluorinated side chain influences peptide backbone geometry and improves bioavailability, making it valuable in the development of pharmaceutical agents. The Fmoc group allows for mild, base-labile protection during solid-phase synthesis, enabling stepwise

Widely used in peptide synthesis, this compound serves as a protected chiral amino acid building block. Its main application lies in the preparation of modified peptides where enhanced metabolic stability and conformational control are required. The difluorinated side chain influences peptide backbone geometry and improves bioavailability, making it valuable in the development of pharmaceutical agents. The Fmoc group allows for mild, base-labile protection during solid-phase synthesis, enabling stepwise assembly of complex peptides. It is particularly useful in research settings focused on structure-activity relationship studies of bioactive peptides.

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