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Indolmycin

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Identification
Molecular formula
C13H12N2O2
CAS number
1072-89-9
IUPAC name
2-imino-3-(1H-indol-3-yl)propanoic acid
State
State

At room temperature, Indolmycin is generally in a solid state. Its crystalline powder form is typical of many small molecule organic compounds, where the rigidity of intermolecular forces maintains it in solid form under ambient conditions.

Melting point (Celsius)
216.00
Melting point (Kelvin)
489.15
Boiling point (Celsius)
359.15
Boiling point (Kelvin)
632.30
General information
Molecular weight
230.25g/mol
Molar mass
230.2520g/mol
Density
1.3500g/cm3
Appearence

Indolmycin appears as a slight yellow crystalline powder. It can be visually characterized by its crystalline structure and slight yellow hue, typical of many organic compounds containing aromatic groups.

Comment on solubility

Solubility of 2-imino-3-(1H-indol-3-yl)propanoic acid

The solubility characteristics of 2-imino-3-(1H-indol-3-yl)propanoic acid, with the molecular formula C13H12N2O2, can be quite intriguing. The presence of both acidic and basic functional groups within the compound often suggests a potential for notable solubility in various solvents. Here are some key points to consider:

  • Polar solvents: Due to the carboxylic acid group, the compound may exhibit increased solubility in polar solvents such as water and alcohol.
  • Non-polar solvents: The indole moiety may lead to some solubility in non-polar organic solvents, though likely at lower levels compared to polar solvents.
  • Temperature effects: As is common with many organic compounds, increased temperature may enhance solubility, allowing for a greater dissolution of the species.

While empirical data on the solubility of 2-imino-3-(1H-indol-3-yl)propanoic acid might be limited, “the nature of the interactions between solute and solvent will ultimately dictate the extent of solubility”. Understanding these interactions can provide insights into its behavior in various chemical contexts.

Interesting facts

Interesting Facts about 2-imino-3-(1H-indol-3-yl)propanoic Acid

2-imino-3-(1H-indol-3-yl)propanoic acid is a fascinating compound that serves as a crucial building block in various biochemical processes. Here are some intriguing insights:

  • Biosynthesis & Derivatives: This compound is part of a class of biogenic compounds that can partake in the biosynthesis of various natural products and derivatives that may have therapeutic potential.
  • Indole Moiety: The presence of the indole ring system in its structure is significant, as indole derivatives are known for numerous biological activities, including antimicrobial and anticancer properties.
  • Role in Biology: Compounds like 2-imino-3-(1H-indol-3-yl)propanoic acid play a role in various enzymatic reactions and are investigated for their potential effects on human health.
  • Research Potential: The compound's multifaceted nature makes it a subject of interest in medicinal chemistry, particularly in the search for new pharmaceutical agents to combat various diseases.
  • Structure-Activity Relationship (SAR): Scientists often explore the SAR of similar compounds, analyzing how changes in structure can lead to different bioactivities, which is a vital area of study in drug design.

As research advances, exploring such compounds could lead to discoveries that enhance our understanding of their biological significance and expand their applications in the field of medicine.

Synonyms
IMINO-TRYPTOPHAN
2-imino-3-(1H-indol-3-yl)propanoic acid
indole-3-pyruvic acid imine
IPA imine
(2z)-2-imino-3-(1h-indol-3-yl)propanoic acid
SCHEMBL4309024
SCHEMBL20211099
CHEBI:59193
CHEBI:90891
2-iminio-3-(indol-3-yl)propanoate
DB02988
2-imino-3-(indol-3-yl)propanoic acid
2-iminio-3-(1H-indol-3-yl)propanoate
NS00068409
C21124
Q27093960