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Catalog Number:
05819
CAS Number:
96594-10-4
Trifluoroacétate de L-alanine 7-amido-4-méthylcoumarine
Purity:
≥ 99 % (HPLC)
Synonym(s):
L-Ala-AMC·TFA
Documents
$60.00 /250 mg
Taille
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Informations sur le produit

L-Alanine 7-amido-4-methylcoumarin trifluoroacetate is a versatile compound widely recognized for its applications in biochemical research and pharmaceutical development. This compound, a derivative of alanine, features a unique coumarin structure that enhances its fluorescence properties, making it an excellent choice for use in fluorescence-based assays and imaging techniques. Its ability to serve as a fluorescent probe allows researchers to study enzyme activity, protein interactions, and cellular processes with high sensitivity and specificity.

In addition to its role in research, L-Alanine 7-amido-4-methylcoumarin trifluoroacetate is also utilized in the synthesis of various bioactive molecules, contributing to advancements in drug discovery and development. Its trifluoroacetate moiety provides stability and solubility, facilitating its incorporation into diverse chemical reactions. This compound stands out for its dual functionality as both a research tool and a building block in synthetic chemistry, making it an invaluable asset for professionals in the fields of biochemistry and medicinal chemistry.

Numéro CAS 
96594-10-4
Formule moléculaire
C13H14N2O3 · C2HO2F3
Poids moléculaire 
360.23
Point de fusion 
199-205º C
Rotation optique 
[a] D 20 = +8,5 ± 1º (c = 1 dans MeOH)
Informations générales
Numéro CAS 
96594-10-4
Formule moléculaire
C13H14N2O3 · C2HO2F3
Poids moléculaire 
360.23
Point de fusion 
199-205º C
Rotation optique 
[a] D 20 = +8,5 ± 1º (c = 1 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

L-Alanine 7-amido-4-methylcoumarin trifluoroacetate is widely utilized in research focused on:

  • Fluorescent Probes: This compound serves as a fluorescent probe in biochemical assays, allowing researchers to track molecular interactions and cellular processes with high sensitivity.
  • Drug Development: Its unique structure makes it valuable in the development of new pharmaceuticals, particularly in targeting specific enzymes or receptors in disease pathways.
  • Bioconjugation: The compound is used in bioconjugation techniques, where it can be attached to biomolecules for enhanced imaging or therapeutic applications, improving drug delivery systems.
  • Analytical Chemistry: It plays a role in analytical chemistry, particularly in the detection and quantification of amino acids and peptides, providing accurate results in protein studies.
  • Research in Enzyme Activity: The compound aids in studying enzyme kinetics and mechanisms, offering insights into metabolic pathways and potential therapeutic targets.

Citations