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Catalog Number:
24655
CAS Number:
1846-76-0
3-carbéthoxycoumarine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ethyl coumarine-3-carboxylate, Ester éthylique de l'acide 2-oxo-2 H -chromène-3-carboxylique
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Product Information

3-Carbethoxycoumarin is a versatile compound known for its unique structure and functional properties, making it an essential building block in organic synthesis and pharmaceutical research. This compound, also recognized as ethyl 2-oxochromene-3-carboxylate, exhibits excellent reactivity, particularly in the formation of coumarin derivatives, which are widely used in the development of various bioactive molecules. Its ability to undergo diverse chemical transformations allows researchers to explore its potential in creating novel compounds with applications in medicinal chemistry, agrochemicals, and dye manufacturing.

The practical applications of 3-Carbethoxycoumarin extend to its use in the synthesis of fluorescent probes and as a precursor in the production of natural product analogs. Its derivatives have shown promise in the fields of anti-inflammatory and anticancer research, highlighting its relevance in drug discovery. Additionally, the compound's favorable solubility and stability make it an attractive option for researchers looking to develop new materials or enhance existing formulations. With its broad range of applications and potential for innovation, 3-Carbethoxycoumarin stands out as a valuable resource for professionals in the chemical and pharmaceutical industries.

Synonyms
Ethyl coumarine-3-carboxylate, Ester éthylique de l'acide 2-oxo-2 H -chromène-3-carboxylique
CAS Number
1846-76-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H10O4
Molecular Weight
218.21
MDL Number
MFCD00016964
PubChem ID
15800
Melting Point
90-96 ?C
Appearance
Cristaux blancs
Conditions
Conserver à 0-8°C
General Information
Synonyms
Ethyl coumarine-3-carboxylate, Ester éthylique de l'acide 2-oxo-2 H -chromène-3-carboxylique
CAS Number
1846-76-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C12H10O4
Molecular Weight
218.21
MDL Number
MFCD00016964
PubChem ID
15800
Melting Point
90-96 ?C
Appearance
Cristaux blancs
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-Carbethoxycoumarin is widely utilized in research focused on:

  • Fluorescent Probes: This compound is used in the development of fluorescent probes for bioimaging applications, allowing researchers to visualize cellular processes in real-time.
  • Pharmaceutical Development: It serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the creation of anticoagulants and anti-inflammatory drugs.
  • Organic Synthesis: The compound is valuable in organic synthesis as a building block for creating more complex molecules, enhancing the efficiency of chemical reactions.
  • Antioxidant Research: It is studied for its potential antioxidant properties, contributing to the development of products aimed at reducing oxidative stress in biological systems.
  • Material Science: 3-Carbethoxycoumarin is explored in the formulation of advanced materials, including coatings and polymers, due to its unique chemical properties.

Citations