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Catalog Number:
26542
CAS Number:
101382-54-1
2-hydroxy-8-méthylquinoléine-3-carbaldéhyde
Purity:
99 - 100 % (HPLC)
Documents
$72.31 /100 mg
Taille
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Product Information

2-Hydroxy-8-methylquinoline-3-carbaldehyde is a versatile compound known for its unique chemical structure and functional properties. This compound, also recognized as 8-methyl-2-oxo-1H-quinoline-3-carbaldehyde, features a hydroxyl group and an aldehyde group, making it an excellent candidate for various applications in organic synthesis and medicinal chemistry. Its ability to act as a building block in the synthesis of complex molecules is particularly valuable in the development of pharmaceuticals and agrochemicals. Researchers have utilized this compound in the synthesis of quinoline derivatives, which are known for their biological activities, including antimicrobial and antitumor properties.

In addition to its synthetic applications, 2-Hydroxy-8-methylquinoline-3-carbaldehyde has shown potential in the field of fluorescence and dye chemistry, where it can be employed as a fluorescent probe due to its unique optical properties. This compound's stability and reactivity make it a preferred choice for researchers looking to explore new pathways in drug discovery and material science. Its multifaceted applications and beneficial properties position it as a valuable asset for professionals in various fields, including pharmaceuticals, materials science, and chemical research.

CAS Number
101382-54-1
Purity
99 - 100 % (HPLC)
Molecular Formula
C 11 H 9 NO 2
Molecular Weight
187.2
MDL Number
MFCD02995894
PubChem ID
788660
Appearance
Poudre jaune
Conditions
Conserver à 0-8°C
General Information
CAS Number
101382-54-1
Purity
99 - 100 % (HPLC)
Molecular Formula
C 11 H 9 NO 2
Molecular Weight
187.2
MDL Number
MFCD02995894
PubChem ID
788660
Appearance
Poudre 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-Hydroxy-8-methylquinoline-3-carbaldehyde is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing anti-cancer and anti-inflammatory drugs.
  • Fluorescent Probes: It is used to create fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time.
  • Analytical Chemistry: The compound is employed in analytical methods for detecting metal ions, making it valuable in environmental monitoring and quality control in industries.
  • Material Science: It plays a role in developing advanced materials, such as polymers and coatings, that require specific optical or chemical properties.
  • Biochemistry Research: This chemical is utilized in studying enzyme activities and interactions, contributing to our understanding of metabolic pathways and disease mechanisms.

Citations