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Identification
Molecular formula
C14H16O3
CAS number
71-44-3
IUPAC name
2-(1-benzyl-5-methoxy-2-methyl-indol-3-yl)acetic acid
State
State

At room temperature, it is typically in the solid state, appearing as a powder.

Melting point (Celsius)
116.00
Melting point (Kelvin)
389.15
Boiling point (Celsius)
413.00
Boiling point (Kelvin)
686.15
General information
Molecular weight
218.28g/mol
Molar mass
218.2700g/mol
Density
1.2200g/cm3
Appearence

It generally appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-(1-benzyl-5-methoxy-2-methyl-indol-3-yl)acetic acid (C14H16O3)

The solubility of 2-(1-benzyl-5-methoxy-2-methyl-indol-3-yl)acetic acid in various solvents is an interesting topic, particularly due to its complex structure. This compound displays moderate solubility characteristics influenced by its functional groups and molecular interactions.

Characteristics of Solubility:

  • Solvent Type: This compound is likely to exhibit higher solubility in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), and acetone compared to polar solvents like water.
  • Temperature Dependency: The solubility can be affected by temperature; generally, increased temperature enhances the solubility of organic compounds.
  • pH Influence: The acidic nature may also play a role, where solubility could vary in different pH environments, suggesting increased solubility in alkaline conditions.

In summary, while we can determine that C14H16O3 is moderately soluble in organic solvents, the specific solubility profile will depend on a variety of factors including temperature, solvent choice, and pH levels, making it a subject of keen interest for further study.

Interesting facts

Interesting Facts about 2-(1-benzyl-5-methoxy-2-methyl-indol-3-yl)acetic acid

This compound belongs to a class of molecules known for their structural complexity and intriguing biological activities. Here are some noteworthy aspects:

  • Unique Structure: The presence of both an indole and a benzyl group in its structure contributes to its distinctive properties, making it a subject of interest in medicinal chemistry.
  • Potential Therapeutic Uses: Compounds containing indole moieties are often linked to various pharmacological effects, including anti-inflammatory, analgesic, and possibly anticancer activities. This has sparked research into its possible applications in drug development.
  • Synthetic Pathways: The synthesis of this compound may involve numerous steps, allowing chemists to explore diverse synthetic routes. This not only aids in understanding reaction mechanisms but also enhances skills in organic synthesis.
  • Interdisciplinary Interest: Researchers from multiple fields, including chemistry, biology, and pharmacology, may collaborate to explore how this compound interacts with biological pathways.
  • Biological Significance: Indole-containing compounds are prevalent in nature and are essential in many biological processes, making them valuable for studies in biochemistry.
  • Research Opportunities: Ongoing studies may reveal new insights into its mechanism of action, helping to identify specific targets in cellular pathways.

In conclusion, 2-(1-benzyl-5-methoxy-2-methyl-indol-3-yl)acetic acid serves as a fascinating example of the intersection between chemical structure and biological activity, providing extensive opportunities for exploration and discovery in the scientific community.

Synonyms
1-benzyl-5-methoxy-2-methyl-1h-indol-3-yl)-acetic acid
59283-35-1
(1-benzyl-5-methoxy-2-methyl-1h-indol-3-yl)acetic acid
5JSR5TT2JJ
CHEMBL148756
NSC-54774
5-methoxy-2-methyl-1-(phenylmethyl)-1H-indole-3-acetic acid
2-(1-benzyl-5-methoxy-2-methylindol-3-yl)acetic acid
I3N
SCHEMBL7963016
DTXSID40274304
ZEKCBTQHDTUHRJ-UHFFFAOYSA-N
NSC54774
BDBM50055737
DB03121
PD007366
NS00068726
1-Benzyl-5-methoxy-2-methyl-3-indoleacetic acid
Q27094071
1-benzyl-5-methoxy-2-methyl-1h-indol-3-yl-acetic acid
(1-Benzyl-5-methoxy-2-methyl-1H-indol-3-yl)-acetic acid
2-(1-benzyl-5-methoxy-2-methyl-1h-indol-3-yl)acetic acid
1H-Indole-3-acetic acid, 5-methoxy-2-methyl-1-(phenylmethyl)-