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Catalog Number:
42766
CAS Number:
817638-68-9
3-Azido-7-hydroxycoumarine
Purity:
≥ 95 % (RMN)
Synonym(s):
3-Azido-7-hydroxy-2 H -chromène-2-one
Temperature Sensitive
Documents
$105.70 /50 mg
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Product Information

3-Azido-7-hydroxycoumarin is a versatile compound known for its unique azido and hydroxy functional groups, which enhance its reactivity and applicability in various fields. This compound is particularly valuable in the synthesis of fluorescent probes and bioorthogonal reactions, making it an essential tool for researchers in biochemistry and molecular biology. Its fluorescent properties allow for effective tracking of biological processes, while the azido group facilitates click chemistry, enabling the conjugation of biomolecules with high specificity and efficiency.

In addition to its applications in research, 3-Azido-7-hydroxycoumarin has potential uses in the development of new therapeutic agents and diagnostic tools. Its ability to serve as a building block in the synthesis of more complex molecules opens up avenues for innovation in drug discovery and development. Researchers and industry professionals can leverage this compound to enhance their studies and create novel applications in the fields of medicinal chemistry and materials science.

Synonyms
3-Azido-7-hydroxy-2 H -chromène-2-one
CAS Number
817638-68-9
Purity
≥ 95 % (RMN)
Molecular Formula
C9H5N3O3
Molecular Weight
203.16
MDL Number
MFCD12924840
PubChem ID
25127608
Melting Point
116 - 122 °C
Appearance
Solide marron
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
3-Azido-7-hydroxy-2 H -chromène-2-one
CAS Number
817638-68-9
Purity
≥ 95 % (RMN)
Molecular Formula
C9H5N3O3
Molecular Weight
203.16
MDL Number
MFCD12924840
PubChem ID
25127608
Melting Point
116 - 122 °C
Appearance
Solide marron
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

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

  • Fluorescent Probes: This compound is used as a fluorescent probe in biological imaging, allowing researchers to visualize cellular processes with high sensitivity and specificity.
  • Drug Development: It serves as a scaffold in medicinal chemistry, aiding in the design of new pharmaceuticals, particularly in targeting cancer cells due to its unique azido group.
  • Photodynamic Therapy: The compound is explored in photodynamic therapy applications, where it can generate reactive oxygen species upon light activation, effectively targeting and destroying tumor cells.
  • Bioconjugation: Its azido functionality enables bioconjugation techniques, facilitating the attachment of biomolecules for targeted delivery systems in drug formulation.
  • Antimicrobial Research: Researchers are investigating its potential antimicrobial properties, making it a candidate for developing new antibacterial agents.

Citations