2,2,2-trifluoro-N-(2((((2(trifluoroacetamido)ethyl)sulfanyl)methyl)sulfanyl)ethyl)acetamide

98%

Reagent Code: #215343
label
Alias Related 118042-46-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 358.32 g/mol
Formula C₉H₁₂O₂F₆N₂S₂
inventory_2 Storage & Handling
Storage 2-8 °C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its fluorinated structure enhances metabolic stability and membrane permeability in drug candidates. Commonly employed in solid-phase peptide synthesis to introduce trifluoroacetyl-protected functional groups. Also utilized in the preparation of enzyme inhibitors and diagnostic probes due to its ability to modulate biological activity through controlled conformational effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿28,080.00
inventory 1g
10-20 days ฿82,800.00
inventory 100mg
10-20 days ฿14,220.00

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2,2,2-trifluoro-N-(2((((2(trifluoroacetamido)ethyl)sulfanyl)methyl)sulfanyl)ethyl)acetamide
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Used as a key intermediate in the synthesis of peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its fluorinated structure enhances metabolic stability and membrane permeability in drug candidates. Commonly employed in solid-phase peptide synthesis to introduce trifluoroacetyl-protected functional groups. Also utilized in the preparation of enzyme inhibitors and diagnostic probes due to its ability to modulate biological activity through controlled conformational effe

Used as a key intermediate in the synthesis of peptide-based pharmaceuticals, particularly in the development of protease inhibitors. Its fluorinated structure enhances metabolic stability and membrane permeability in drug candidates. Commonly employed in solid-phase peptide synthesis to introduce trifluoroacetyl-protected functional groups. Also utilized in the preparation of enzyme inhibitors and diagnostic probes due to its ability to modulate biological activity through controlled conformational effects.

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