(2R,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(benzyloxy)butanoic acid

≥95%

Reagent Code: #50252
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CAS Number 131545-63-6

science Other reagents with same CAS 131545-63-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 431.48 g/mol
Formula C₂₆H₂₅NO₅
badge Registry Numbers
MDL Number MFCD00237033
thermostat Physical Properties
Boiling Point 643.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block in solid-phase peptide synthesis (SPPS), where the fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino functionality. The benzyloxy group protects the hydroxyl side chain, ensuring selective reactivity during the coupling process. Its application is crucial in producing peptides with high purity and specificity, particularly in pharmaceutical research and drug development. The compound’s structure allows for efficient deprotection and coupling steps, making it a valuable tool in synthesizing complex peptides and proteins.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿918.00
inventory 100mg
10-20 days ฿360.00
inventory 5g
10-20 days ฿2,934.00
inventory 250mg
10-20 days ฿387.00

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(2R,3S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(benzyloxy)butanoic acid
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This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block in solid-phase peptide synthesis (SPPS), where the fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino functionality. The benzyloxy group protects the hydroxyl side chain, ensuring selective reactivity during the coupling process. Its application is crucial in producing peptides with high purity and specificity, particularly in pharmaceutical research and drug development. The compound’s structure allows for efficient deprotection and coupling steps, making it a valuable tool in synthesizing complex peptides and proteins.
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