N-(2,2,2-Trifluoroacetyl)-L-valine triethylamine salt

97%

Reagent Code: #219376
label
Alias Related CAS Number: 349-00-8,N-(2,2,2-trifluoroacetyl)-L-valine triethylamine salt, L-trifluoroacetylvaline triethylamine salt, Trifluoroacetyl-L-valine triethylamine salt

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.34 g/mol
Formula C₁₃H₂₅F₃N₂O₃
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral derivatizing agent in the synthesis of pharmaceuticals, particularly in asymmetric synthesis and resolution of enantiomers. Its trifluoroacetyl group enhances reactivity and selectivity in coupling reactions, making it valuable in the preparation of peptide mimetics and beta-amino acids. Commonly employed in liquid chromatography and NMR spectroscopy for enantiomeric purity analysis due to the distinct signals provided by the fluorine atoms. Also utilized in agrochemical and fine chemical industries where stereochemical control is critical.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,880.00
inventory 5g
10-20 days ฿5,910.00
inventory 25g
10-20 days ฿19,300.00

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N-(2,2,2-Trifluoroacetyl)-L-valine triethylamine salt
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Used as a chiral derivatizing agent in the synthesis of pharmaceuticals, particularly in asymmetric synthesis and resolution of enantiomers. Its trifluoroacetyl group enhances reactivity and selectivity in coupling reactions, making it valuable in the preparation of peptide mimetics and beta-amino acids. Commonly employed in liquid chromatography and NMR spectroscopy for enantiomeric purity analysis due to the distinct signals provided by the fluorine atoms. Also utilized in agrochemical and fine chemica

Used as a chiral derivatizing agent in the synthesis of pharmaceuticals, particularly in asymmetric synthesis and resolution of enantiomers. Its trifluoroacetyl group enhances reactivity and selectivity in coupling reactions, making it valuable in the preparation of peptide mimetics and beta-amino acids. Commonly employed in liquid chromatography and NMR spectroscopy for enantiomeric purity analysis due to the distinct signals provided by the fluorine atoms. Also utilized in agrochemical and fine chemical industries where stereochemical control is critical.

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