(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propanoic acid

95%

Reagent Code: #231451
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CAS Number 517905-88-3

science Other reagents with same CAS 517905-88-3

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

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its structure incorporates both a fluorenylmethyloxycarbonyl (Fmoc) protecting group and a trifluoromethylphenyl moiety, making it valuable in solid-phase peptide synthesis and asymmetric synthesis. The compound is especially useful in creating enantiomerically pure compounds for drug discovery due to its stereochemical integrity and functional group compatibility. It also serves as a key intermediate in the preparation of enzyme inhibitors where the trifluoromethyl group enhances metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,690.00
inventory 250mg
10-20 days ฿4,780.00
inventory 1g
10-20 days ฿11,680.00
inventory 5g
10-20 days ฿48,490.00
inventory 10g
10-20 days ฿56,600.00
(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(trifluoromethyl)phenyl)propanoic acid
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its structure incorporates both a fluorenylmethyloxycarbonyl (Fmoc) protecting group and a trifluoromethylphenyl moiety, making it valuable in solid-phase peptide synthesis and asymmetric synthesis. The compound is especially useful in creating enantiomerically pure compounds for drug discovery due to its stereochemical integrity and funct

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its structure incorporates both a fluorenylmethyloxycarbonyl (Fmoc) protecting group and a trifluoromethylphenyl moiety, making it valuable in solid-phase peptide synthesis and asymmetric synthesis. The compound is especially useful in creating enantiomerically pure compounds for drug discovery due to its stereochemical integrity and functional group compatibility. It also serves as a key intermediate in the preparation of enzyme inhibitors where the trifluoromethyl group enhances metabolic stability and binding affinity.

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