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Catalog Number:
42778
CAS Number:
6093-71-6
7-hydroxycoumarine-3-carboxylate d'éthyle
Purity:
≥ 98% (CG)
Synonym(s):
Ester éthylique de l'acide 7-hydroxycoumarine-3-carboxylique, Ombelliférone-3-carboxylate d'éthyle, Ester éthylique de l'acide umbelliférone-3-carboxylique
Documents
$262.59 /200 mg
Taille
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Informations sur le produit

Ethyl 7-hydroxycoumarin-3-carboxylate is a versatile compound known for its unique properties and applications in various fields. This compound, a derivative of coumarin, exhibits excellent fluorescence and is widely utilized in the development of fluorescent probes and dyes. Its ability to absorb light and emit fluorescence makes it particularly valuable in biological imaging and analytical chemistry, where it can be used to track cellular processes or detect specific biomolecules. Additionally, its structure allows for potential applications in pharmaceuticals, particularly in the design of new drugs targeting various diseases due to its bioactive properties.

Researchers and industry professionals appreciate Ethyl 7-hydroxycoumarin-3-carboxylate for its stability and ease of modification, enabling the synthesis of derivatives tailored for specific applications. Its low toxicity profile further enhances its appeal in both laboratory and industrial settings. With its diverse applications ranging from fluorescence-based assays to potential therapeutic uses, this compound stands out as a significant tool for innovation in scientific research and product development.

Numéro CAS 
6093-71-6
Formule moléculaire
C12H10O5
Poids moléculaire 
234.21
Point de fusion 
170 - 174 °C
Informations générales
Numéro CAS 
6093-71-6
Formule moléculaire
C12H10O5
Poids moléculaire 
234.21
Point de fusion 
170 - 174 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Ethyl 7-hydroxycoumarin-3-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is often explored for its potential therapeutic properties, particularly in the development of anti-inflammatory and anticoagulant medications.
  • Fluorescent Probes: Its unique structure allows it to be used as a fluorescent probe in biochemical assays, aiding researchers in tracking cellular processes and interactions.
  • Cosmetic Formulations: The compound is incorporated into skincare products for its antioxidant properties, helping to protect the skin from oxidative stress and improve overall skin health.
  • Food Industry: It serves as a natural flavoring agent and preservative, enhancing the shelf life and safety of various food products while contributing to flavor profiles.
  • Environmental Monitoring: Ethyl 7-hydroxycoumarin-3-carboxylate is used in environmental studies to detect and quantify pollutants, providing valuable data for ecological assessments.

Citations