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2-acetyl-3-methyl-1,5,6,7-tetrahydroindol-4-one

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Identification
Molecular formula
C13H15NO2
CAS number
31947-47-4
IUPAC name
2-acetyl-3-methyl-1,5,6,7-tetrahydroindol-4-one
State
State
At room temperature, this compound is present in solid state, most likely as a crystalline solid or powder.
Melting point (Celsius)
144.00
Melting point (Kelvin)
417.15
Boiling point (Celsius)
533.15
Boiling point (Kelvin)
806.30
General information
Molecular weight
205.27g/mol
Molar mass
205.2480g/mol
Density
1.1560g/cm3
Appearence

2-acetyl-3-methyl-1,5,6,7-tetrahydroindol-4-one typically appears as a crystalline solid. The compound may be off-white to pale yellow in color, reflecting its organic nature and composition.

Comment on solubility

Solubility of 2-acetyl-3-methyl-1,5,6,7-tetrahydroindol-4-one

The solubility of 2-acetyl-3-methyl-1,5,6,7-tetrahydroindol-4-one is influenced by several factors, making it a compound with interesting characteristics in various solvents.

  • Solvent Polarity: This compound tends to exhibit different solubility patterns depending on the polarity of the solvent. Generally, it is more soluble in nonpolar solvents due to its hydrophobic structure.
  • Temperature Effects: Increasing the temperature can often enhance the solubility of solid compounds. For 2-acetyl-3-methyl-1,5,6,7-tetrahydroindol-4-one, research indicates an increase in solubility with rising temperature.
  • Functional Group Impact: The presence of the acetyl functional group can provide some degree of solubility in polar solvents, although it may be limited compared to more hydrophilic compounds.

In summary, solubility factors to consider for 2-acetyl-3-methyl-1,5,6,7-tetrahydroindol-4-one include solvent polarity, temperature, and functional group composition. Understanding these variables is essential for effectively utilizing this compound in various chemical applications.

Interesting facts

Interesting Facts about 2-acetyl-3-methyl-1,5,6,7-tetrahydroindol-4-one

2-acetyl-3-methyl-1,5,6,7-tetrahydroindol-4-one, often abbreviated as AMT, is a fascinating compound with a variety of intriguing properties and applications. Here are some notable aspects:

  • Origin and Structure: This compound belongs to the indole family, which is known for its complex cyclic structure. Indoles play a significant role in many biological systems, making compounds like AMT points of interest for medicinal chemistry.
  • Biological Activity: Research has indicated that derivatives of AMT may exhibit various pharmacological effects, including anti-inflammatory and antioxidant properties. This makes it a subject of interest in drug discovery.
  • Potential Applications: AMT is being explored for its potential use in:
    • Pharmaceuticals: Possible applications in developing new therapeutic agents.
    • Agricultural Chemistry: Investigating its roles in plant growth regulators.
  • Analytical interest: Its unique structure makes AMT a compound of interest in analytical chemistry, particularly in studies focusing on spectroscopy and chromatography.
  • Complex Synthesis: The synthesis of 2-acetyl-3-methyl-1,5,6,7-tetrahydroindol-4-one is a challenge, often requiring innovative strategies to construct its multi-ring architecture effectively.

As chemists continue to explore the potential of compounds like AMT, it becomes increasingly clear that these connections between structure and function are vital in formulating new materials and understanding biological processes. Each study on AMT opens doors to numerous possibilities, underscoring the importance of this compound in both chemistry and related fields.

Synonyms
BRN 1528849
INDOL-4(5H)-ONE, 2-ACETYL-6,7-DIHYDRO-3-METHYL-
14006-80-5
2-Acetyl-6,7-dihydro-3-methyl-indol-4(5H)-one
DTXSID00161221
5-21-10-00203 (Beilstein Handbook Reference)
DTXCID9083712
AKOS022505634
ST097490
2-acetyl-3-methyl-4-oxo-5,6,7-trihydroindole
AG-690/40719690
2-acetyl-3-methyl-1,5,6,7-tetrahydro-4H-indol-4-one