(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(trifluoromethyl)phenyl)propanoic acid

95%

Reagent Code: #231450
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CAS Number 517905-87-2

science Other reagents with same CAS 517905-87-2

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inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of peptidomimetics and pharmaceuticals. Its structure allows incorporation into peptide chains to modify stability, selectivity, and binding properties. Commonly employed in solid-phase peptide synthesis due to the Fmoc group, which enables mild deprotection conditions. The trifluoromethylphenyl moiety enhances lipophilicity and metabolic stability, making it valuable in drug design for improved pharmacokinetics. Also utilized in research for creating enzyme inhibitors and receptor ligands.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,680.00
inventory 250mg
10-20 days ฿4,510.00
inventory 1g
10-20 days ฿11,850.00
inventory 5g
10-20 days ฿49,920.00
inventory 10g
10-20 days ฿56,600.00

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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-(trifluoromethyl)phenyl)propanoic acid
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of peptidomimetics and pharmaceuticals. Its structure allows incorporation into peptide chains to modify stability, selectivity, and binding properties. Commonly employed in solid-phase peptide synthesis due to the Fmoc group, which enables mild deprotection conditions. The trifluoromethylphenyl moiety enhances lipophilicity and metabolic stability, making it valuable in drug design for improved

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of peptidomimetics and pharmaceuticals. Its structure allows incorporation into peptide chains to modify stability, selectivity, and binding properties. Commonly employed in solid-phase peptide synthesis due to the Fmoc group, which enables mild deprotection conditions. The trifluoromethylphenyl moiety enhances lipophilicity and metabolic stability, making it valuable in drug design for improved pharmacokinetics. Also utilized in research for creating enzyme inhibitors and receptor ligands.

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