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Catalog Number:
44447
CAS Number:
2199-90-8
6-Bromocoumarine-3-carboxylate d'éthyle
Purity:
≥ 98% (CG)
Synonym(s):
Ester éthylique de l'acide 6-bromocoumarine-3-carboxylique
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$181.97 /5G
Taille
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Informations sur le produit

Ethyl 6-Bromocoumarin-3-carboxylate is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This compound is recognized for its unique bromine substituent, which enhances its reactivity and makes it an ideal building block for the development of various bioactive molecules. Its structural features allow for applications in the synthesis of coumarin derivatives, which are known for their diverse biological activities, including anti-inflammatory, anticoagulant, and antimicrobial properties. Researchers often leverage this compound in the design of fluorescent probes and as intermediates in the production of pharmaceuticals, thereby expanding its utility in drug discovery and development.

In addition to its synthetic applications, Ethyl 6-Bromocoumarin-3-carboxylate serves as a valuable tool in photochemistry and material science, where it can be used to create light-emitting materials and sensors. Its ability to undergo various chemical transformations makes it a preferred choice for chemists looking to innovate in the fields of organic electronics and photonic devices. With its broad range of applications and significant advantages over similar compounds, Ethyl 6-Bromocoumarin-3-carboxylate stands out as a crucial component for researchers and industry professionals aiming to push the boundaries of chemical synthesis and application.

Numéro CAS 
2199-90-8
Formule moléculaire
C12H9BrO4
Poids moléculaire 
297.1
Point de fusion 
168 - 172 °C
Informations générales
Numéro CAS 
2199-90-8
Formule moléculaire
C12H9BrO4
Poids moléculaire 
297.1
Point de fusion 
168 - 172 °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 6-Bromocoumarin-3-carboxylate is widely utilized in research focused on:

  • Fluorescent Probes: This compound is often used to develop fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time.
  • Synthetic Chemistry: It serves as an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, providing a versatile building block for complex molecules.
  • Photochemistry: The compound is employed in photochemical studies, particularly in the development of light-activated drugs, enhancing targeted therapy options in medicine.
  • Antimicrobial Research: Ethyl 6-Bromocoumarin-3-carboxylate has shown potential antimicrobial properties, making it a candidate for developing new antibacterial agents.
  • Natural Product Synthesis: It is used in the synthesis of coumarin derivatives, which are important in the fragrance industry and as bioactive compounds in herbal medicine.

Citations