(R)-3-((tert-Butoxycarbonyl)amino)-4-(4-(trifluoromethyl)phenyl)butanoic acid

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Reagent Code: #104257
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CAS Number 269726-77-4

science Other reagents with same CAS 269726-77-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 347.33 g/mol
Formula C₁₆H₂₀F₃NO₄
badge Registry Numbers
MDL Number MFCD01860972
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a trifluoromethylphenyl moiety, makes it valuable for developing peptides and small-molecule drugs. The Boc group is often employed to protect amines during multi-step synthetic processes, ensuring selective reactions. Additionally, the trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds, making it useful in the design of potential therapeutic agents, particularly in areas like enzyme inhibition or receptor modulation. Its application is also seen in the preparation of chiral compounds, leveraging its stereocenter for asymmetric synthesis in drug development.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,620.00
inventory 100mg
10-20 days ฿7,092.00

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(R)-3-((tert-Butoxycarbonyl)amino)-4-(4-(trifluoromethyl)phenyl)butanoic acid
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This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a trifluoromethylphenyl moiety, makes it valuable for developing peptides and small-molecule drugs. The Boc group is often employed to protect amines during multi-step synthetic processes, ensuring selective reactions. Additionally, the trifluoromethyl group enhances the biologica

This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of more complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a trifluoromethylphenyl moiety, makes it valuable for developing peptides and small-molecule drugs. The Boc group is often employed to protect amines during multi-step synthetic processes, ensuring selective reactions. Additionally, the trifluoromethyl group enhances the biological activity and metabolic stability of the resulting compounds, making it useful in the design of potential therapeutic agents, particularly in areas like enzyme inhibition or receptor modulation. Its application is also seen in the preparation of chiral compounds, leveraging its stereocenter for asymmetric synthesis in drug development.

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