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Catalog Number:
39725
CAS Number:
1256259-14-9
4-(Bromomethyl)-7-(diethylamino)coumarin
Purity:
≥ 97% (HPLC)
Documents
$418.03 /200MG
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Product Information

4-(Bromomethyl)-7-(diethylamino)coumarin is a versatile compound widely recognized for its applications in fluorescence microscopy and as a fluorescent probe in biological research. This compound features a unique bromomethyl group that enhances its reactivity, making it an excellent choice for labeling biomolecules. Its diethylamino group contributes to its solubility in organic solvents, facilitating its use in various experimental setups. Researchers utilize this compound for tracking cellular processes, studying protein interactions, and developing biosensors due to its strong fluorescence properties.

In addition to its utility in biological applications, 4-(Bromomethyl)-7-(diethylamino)coumarin is also employed in the development of advanced materials and coatings. Its ability to emit light upon excitation makes it suitable for applications in optoelectronics and photonic devices. The compound's stability and ease of functionalization allow for the creation of tailored materials that meet specific performance criteria in diverse industrial applications. With its broad range of uses and unique properties, this compound is an essential tool for researchers and industry professionals alike.

CAS Number
1256259-14-9
Purity
≥ 97% (HPLC)
Molecular Formula
C14H16BrNO2
Molecular Weight
310.19
MDL Number
MFCD31618098
PubChem ID
132274938
Appearance
Light yellow to brown crystalline powder
Conditions
Store at RT
General Information
CAS Number
1256259-14-9
Purity
≥ 97% (HPLC)
Molecular Formula
C14H16BrNO2
Molecular Weight
310.19
MDL Number
MFCD31618098
PubChem ID
132274938
Appearance
Light yellow to brown 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

4-(Bromomethyl)-7-(diethylamino)coumarin is widely utilized in research focused on:

  • Fluorescent Probes: This compound serves as an effective fluorescent probe in biological imaging, allowing researchers to visualize cellular processes in real-time.
  • Photodynamic Therapy: Its properties make it suitable for applications in photodynamic therapy, where it can be used to target and destroy cancer cells when activated by light.
  • Organic Synthesis: The compound is valuable in organic synthesis, particularly in the production of other coumarin derivatives, which have diverse applications in pharmaceuticals and agrochemicals.
  • Sensor Development: It is employed in the development of chemical sensors due to its ability to respond to specific environmental changes, making it useful in monitoring applications.
  • Bioconjugation: The bromomethyl group allows for bioconjugation, facilitating the attachment of this compound to biomolecules for targeted drug delivery systems.

Citations