(S)-2-((tert-Butoxycarbonyl)amino)-4, 4, 4-trifluorobutanoic acid

98%

Reagent Code: #236517
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CAS Number 181128-25-6

science Other reagents with same CAS 181128-25-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.21 g/mol
Formula C₉H₁₄F₃NO₄
badge Registry Numbers
MDL Number MFCD08532484
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in drug design. The Boc-protected amine allows for selective deprotection and coupling in peptide-like structures, enabling controlled assembly of complex molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its steric and electronic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,430.00
inventory 250mg
10-20 days ฿20,160.00
inventory 1g
10-20 days ฿53,940.00

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(S)-2-((tert-Butoxycarbonyl)amino)-4, 4, 4-trifluorobutanoic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in drug design. The Boc-protected amine allows for selective deprotection and coupling in peptide-like structures, enabling controlled assembly of complex molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies du

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in drug design. The Boc-protected amine allows for selective deprotection and coupling in peptide-like structures, enabling controlled assembly of complex molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its steric and electronic properties.

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