N-Boc-2-(4-trifluoromethylphenyl)-DL-glycine

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Reagent Code: #58283
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CAS Number 847147-40-4

science Other reagents with same CAS 847147-40-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.28 g/mol
Formula C₁₄H₁₆F₃NO₄
badge Registry Numbers
MDL Number MFCD07388841
thermostat Physical Properties
Boiling Point 416.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This compound is primarily used in the synthesis of pharmaceuticals and organic compounds, particularly as an intermediate in the production of more complex molecules. Its Boc (tert-butoxycarbonyl) protecting group makes it valuable in peptide synthesis, where it safeguards the amino group during reactions. The trifluoromethylphenyl group enhances the compound's stability and can influence the biological activity of the final product, making it useful in the development of drugs targeting specific receptors or enzymes. It is often employed in research and development for creating potential therapeutic agents, especially in areas like oncology, neurology, and anti-inflammatory treatments. Additionally, its unique structure allows for further functionalization, enabling chemists to explore diverse chemical modifications for tailored applications.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿40,500.00

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N-Boc-2-(4-trifluoromethylphenyl)-DL-glycine
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This compound is primarily used in the synthesis of pharmaceuticals and organic compounds, particularly as an intermediate in the production of more complex molecules. Its Boc (tert-butoxycarbonyl) protecting group makes it valuable in peptide synthesis, where it safeguards the amino group during reactions. The trifluoromethylphenyl group enhances the compound's stability and can influence the biological activity of the final product, making it useful in the development of drugs targeting specific recept

This compound is primarily used in the synthesis of pharmaceuticals and organic compounds, particularly as an intermediate in the production of more complex molecules. Its Boc (tert-butoxycarbonyl) protecting group makes it valuable in peptide synthesis, where it safeguards the amino group during reactions. The trifluoromethylphenyl group enhances the compound's stability and can influence the biological activity of the final product, making it useful in the development of drugs targeting specific receptors or enzymes. It is often employed in research and development for creating potential therapeutic agents, especially in areas like oncology, neurology, and anti-inflammatory treatments. Additionally, its unique structure allows for further functionalization, enabling chemists to explore diverse chemical modifications for tailored applications.

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