5-(Dimethylamino)-1H-indole-3-carbaldehyde

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Identification

Molecular formula
C11H12N2O
CAS Number
114223-69-3
IUPAC Name
5-(dimethylamino)-1H-indole-3-carbaldehyde
Molecular Weight
202.24g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2400g/cm3
Synonyms
3-Formyl-5-dimethylamino indole
Interesting facts

Interesting Facts about 5-(dimethylamino)-1H-indole-3-carbaldehyde

5-(dimethylamino)-1H-indole-3-carbaldehyde, often referred to as an important intermediate in organic synthesis, boasts an intriguing structure that combines indole’s aromaticity with an aldehyde functional group. Here are some captivating points to consider:

  • Role in Research: This compound is widely recognized in the field of medicinal chemistry for its role in the synthesis of various pharmaceuticals and organic compounds.
  • Fluorescent Properties: It exhibits interesting fluorescent properties, making it a potential candidate for use in bioimaging and as a fluorescent probe.
  • Reactivity: The aldehyde group plays a crucial role in its reactivity, allowing for further functionalization and derivatization, paving the way for the creation of even more complex structures.
  • Biological Activity: Compounds with similar structures have been investigated for their biological activity, including potential applications as anticancer agents.
  • Electronic Properties: The presence of the dimethylamino group contributes to its electronic properties, affecting how it interacts with light and other chemicals.

This compound is a testament to the beauty of chemical diversity and the innovative possibilities within the realm of organic chemistry. As one delves deeper into the study of 5-(dimethylamino)-1H-indole-3-carbaldehyde, the layers of its importance in both academic research and practical applications become increasingly evident. Truly, it's a compound that embodies the intersection of creativity and science!

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