Tryptophan methyl ester

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Identification

Molecular formula
C14H15NO2
CAS Number
166652-46-6
IUPAC Name
2-(4,7-dimethyl-1H-indol-3-yl)acetic acid
Molecular Weight
217.27g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3000g/cm3
Synonyms
6306-14-5
Interesting facts

Interesting Facts about 2-(4,7-dimethyl-1H-indol-3-yl)acetic acid

2-(4,7-dimethyl-1H-indol-3-yl)acetic acid is a compound that may not be widely known, but it holds intriguing features that pique the interest of chemists and biochemists alike. This compound belongs to the indole family, a well-studied class of compounds that plays a vital role in various biological processes.

Biological Significance

One of the most fascinating aspects of 2-(4,7-dimethyl-1H-indol-3-yl)acetic acid is its potential biological activity. Indoles are often found in many natural products, and their derivatives can exhibit notable pharmacological properties. Here are some key points:

  • Antioxidant Properties: Many indole derivatives possess the ability to scavenge free radicals, suggesting potential protective effects against oxidative stress.
  • Roles in Neurochemistry: Compounds featuring the indole structure, such as serotonin, are vital in neurotransmission.
  • Potential Therapeutic Applications: Due to its unique structure, compounds like 2-(4,7-dimethyl-1H-indol-3-yl)acetic acid might be explored for their efficacy in drug development, particularly in cancer and neurological disorders.

Chemical Structure and Features

The structural configuration of 2-(4,7-dimethyl-1H-indol-3-yl)acetic acid presents an interesting blend of aromatic and functional groups. This contributes to its reactivity and accommodating interactions in various chemical reactions. A few noteworthy features include:

  • Indole Framework: The indole structure lends a rich source for bonding and reactivity, essential for synthesizing various derivatives.
  • Methyl Substitution: The presence of dimethyl groups modulates the compound's electronic properties and steric effects, critical for both reactivity and biological interactions.

Conclusion

In conclusion, 2-(4,7-dimethyl-1H-indol-3-yl)acetic acid is more than just a name; it represents a world of chemical potential, especially in the realm of medicinal chemistry. As research continues, this compound might unveil further secrets, lending itself to innovative applications in science and medicine.

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