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Catalog Number:
42787
CAS Number:
28705-46-6
Ethyl 7-(Diethylamino)coumarin-3-carboxylate
Purity:
≥ 98% (GC)
Synonym(s):
7-(Diethylamino)coumarin-3-carboxylic acid ethyl ester
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Product Information

Ethyl 7-(Diethylamino)coumarin-3-carboxylate is a versatile compound known for its vibrant fluorescence and significant applications in various fields, including biochemistry and materials science. This compound, also recognized by its synonyms such as 7-(Diethylamino)coumarin-3-carboxylic acid ethyl ester, is particularly valued for its role as a fluorescent probe in biological imaging and as a dye in laser applications. Its unique structure allows it to exhibit strong absorption and emission properties, making it ideal for use in fluorescence microscopy and flow cytometry, where precise visualization of biological processes is crucial.

In addition to its applications in research, Ethyl 7-(Diethylamino)coumarin-3-carboxylate is utilized in the development of advanced materials, including sensors and organic light-emitting diodes (OLEDs). The compound's stability and efficiency in light emission provide a competitive edge over similar compounds, enhancing its desirability in both academic and industrial settings. Researchers and professionals can leverage this compound to achieve superior results in their projects, particularly in fields requiring high sensitivity and specificity in detection methods.

Synonyms
7-(Diethylamino)coumarin-3-carboxylic acid ethyl ester
CAS Number
28705-46-6
Purity
≥ 98% (GC)
Molecular Formula
C16H19NO4
Molecular Weight
289.33
MDL Number
MFCD00227484
PubChem ID
120014
Melting Point
84 - 88 °C
Appearance
Light yellow to amber to dark green crystalline powder
Conditions
Store at RT
General Information
Synonyms
7-(Diethylamino)coumarin-3-carboxylic acid ethyl ester
CAS Number
28705-46-6
Purity
≥ 98% (GC)
Molecular Formula
C16H19NO4
Molecular Weight
289.33
MDL Number
MFCD00227484
PubChem ID
120014
Melting Point
84 - 88 °C
Appearance
Light yellow to amber to dark green crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 7-(Diethylamino)coumarin-3-carboxylate is widely utilized in research focused on:

  • Fluorescent Probes: This compound is often used as a fluorescent probe in biological imaging, allowing researchers to visualize cellular processes in real-time due to its strong fluorescence properties.
  • Photodynamic Therapy: In the medical field, it serves as a photosensitizer in photodynamic therapy, a treatment that uses light to activate a drug that kills cancer cells, demonstrating effectiveness in targeting tumors.
  • Organic Synthesis: It plays a significant role in organic synthesis as a building block for creating more complex molecules, particularly in the development of new pharmaceuticals and agrochemicals.
  • Analytical Chemistry: The compound is used in analytical chemistry for the detection and quantification of various substances, leveraging its unique spectral properties for sensitive measurements.
  • Biochemical Research: It is applied in biochemical research to study enzyme activities and interactions, providing insights into metabolic pathways and potential drug targets.

Citations