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Catalog Number:
24679
CAS Number:
61424-76-8
2-Amino-3-formylchromone
Purity:
≥ 99 % (HPLC)
Synonym(s):
2-Amino-4-oxo-4 H -1-benzopyran-3-carboxaldéhyde, 2-Amino-4-oxo-4 H -chromène-3-carbaldéhyde
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Product Information

2-Amino-3-formylchromone is a versatile compound recognized for its unique structural features and functional properties, making it a valuable asset in various fields of research and industry. This compound, a derivative of chromone, exhibits significant potential in the synthesis of biologically active molecules, particularly in the development of pharmaceuticals and agrochemicals. Its aldehyde functional group allows for easy derivatization, facilitating the creation of a wide range of derivatives that can be tailored for specific applications.

Researchers have utilized 2-Amino-3-formylchromone in the synthesis of novel anti-cancer agents and anti-inflammatory drugs, showcasing its relevance in medicinal chemistry. Additionally, its ability to act as a fluorescent probe opens avenues for applications in bioimaging and sensor technology. The compound's stability and reactivity make it an attractive choice for organic synthesis, providing a reliable building block for complex molecular architectures. With its diverse applications and the potential for further exploration, 2-Amino-3-formylchromone stands out as a compound of interest for professionals in chemical research and development.

Synonyms
2-Amino-4-oxo-4 H -1-benzopyran-3-carboxaldéhyde, 2-Amino-4-oxo-4 H -chromène-3-carbaldéhyde
CAS Number
61424-76-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H7N O 3
Molecular Weight
189.17
MDL Number
MFCD00191735
PubChem ID
735928
Melting Point
254 - 258 ?C
Appearance
Solide amorphe jaune
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
2-Amino-4-oxo-4 H -1-benzopyran-3-carboxaldéhyde, 2-Amino-4-oxo-4 H -chromène-3-carbaldéhyde
CAS Number
61424-76-8
Purity
≥ 99 % (HPLC)
Molecular Formula
C10H7N O 3
Molecular Weight
189.17
MDL Number
MFCD00191735
PubChem ID
735928
Melting Point
254 - 258 ?C
Appearance
Solide amorphe jaune
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

2-Amino-3-formylchromone is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a precursor in the synthesis of various bioactive molecules, particularly in the development of anti-cancer agents and anti-inflammatory drugs, enhancing therapeutic efficacy.
  • Fluorescent Probes: It is employed in creating fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high specificity and sensitivity.
  • Organic Synthesis: The compound is a valuable building block in organic chemistry, facilitating the construction of complex molecular architectures used in material science and nanotechnology.
  • Analytical Chemistry: It is used in the development of analytical methods for detecting metal ions, providing a reliable approach for environmental monitoring and quality control in various industries.
  • Natural Product Research: This chemical plays a role in the study of natural products, aiding in the extraction and characterization of compounds from plants that may have medicinal properties.

Citations