(R)-2-Amino-5,5,5-Trifluoropentanamide Hydrochloride

95%

Reagent Code: #231638
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CAS Number 1146699-58-2

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.59 g/mol
Formula C₅H₁₀ClF₃N₂O
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of biologically active compounds, particularly as a chiral building block in pharmaceutical development. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in designing protease inhibitors and other therapeutic agents. Commonly employed in the preparation of peptide mimetics due to its amide and amino functionalities, which allow for selective coupling reactions. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies, especially in CNS-targeted drugs where fluorination improves blood-brain barrier penetration.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,410.00

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(R)-2-Amino-5,5,5-Trifluoropentanamide Hydrochloride
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Used in the synthesis of biologically active compounds, particularly as a chiral building block in pharmaceutical development. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in designing protease inhibitors and other therapeutic agents. Commonly employed in the preparation of peptide mimetics due to its amide and amino functionalities, which allow for selective coupling reactions. Also utilized in medicinal chemistry research for structure-activity re

Used in the synthesis of biologically active compounds, particularly as a chiral building block in pharmaceutical development. Its trifluoromethyl group enhances metabolic stability and membrane permeability, making it valuable in designing protease inhibitors and other therapeutic agents. Commonly employed in the preparation of peptide mimetics due to its amide and amino functionalities, which allow for selective coupling reactions. Also utilized in medicinal chemistry research for structure-activity relationship (SAR) studies, especially in CNS-targeted drugs where fluorination improves blood-brain barrier penetration.

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