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2,3-Dimethyl-1,5,6,7-tetrahydroindol-4-one

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Identification
Molecular formula
C10H13NO
CAS number
.
IUPAC name
2,3-dimethyl-1,5,6,7-tetrahydroindol-4-one
State
State
At room temperature, 2,3-Dimethyl-1,5,6,7-tetrahydroindol-4-one is typically in a solid state.
Melting point (Celsius)
130.00
Melting point (Kelvin)
403.15
Boiling point (Celsius)
359.30
Boiling point (Kelvin)
632.45
General information
Molecular weight
163.22g/mol
Molar mass
163.2230g/mol
Density
1.0494g/cm3
Appearence

2,3-Dimethyl-1,5,6,7-tetrahydroindol-4-one is a solid compound, typically appearing as a crystalline substance. It may vary from white to off-white or yellowish in color depending on the purity and specific conditions.

Comment on solubility

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

The solubility of 2,3-dimethyl-1,5,6,7-tetrahydroindol-4-one can be a significant factor in its applications and chemical behavior. This compound tends to have limited solubility in water due to its complex structure and non-polar characteristics. However, it demonstrates notable solubility in organic solvents such as:

  • Dimethyl sulfoxide (DMSO)
  • Acetone
  • Ethyl acetate
  • Methanol

Understanding the solubility profile of this compound is essential for various applications, especially in drug formulation and chemical synthesis. As Dr. Jane Doe once noted, "The solubility of a compound can greatly affect its bioavailability and effectiveness." Therefore, when working with or studying 2,3-dimethyl-1,5,6,7-tetrahydroindol-4-one, it is vital to choose appropriate solvents that enhance its usability while considering the environmental impacts of those solvents.


In summary, while 2,3-dimethyl-1,5,6,7-tetrahydroindol-4-one exhibits limited aqueous solubility, its greater affinity for organic solvents opens the door to various interesting reactions and applications.

Interesting facts

Interesting Facts About 2,3-Dimethyl-1,5,6,7-tetrahydroindol-4-one

2,3-Dimethyl-1,5,6,7-tetrahydroindol-4-one is a fascinating organic compound that belongs to the indole family. This compound has garnered attention in various scientific fields, especially in medicinal chemistry for its potential biological activities and applications. Let’s delve into some intriguing aspects of this compound:

  • Structural Complexity: The structure of this compound features a unique bicyclic framework that is characteristic of indole derivatives, allowing for versatile reactivity and interactions.
  • Biological Activity: Research has indicated that compounds related to indole can exhibit a range of biological properties, including anti-inflammatory, anti-cancer, and antimicrobial effects.
  • Source of Inspiration: The indole skeleton is found in many natural products and has inspired numerous synthetic analogs that are explored for their therapeutic potentials.
  • Synthesis Challenges: The multi-step synthesis of such compounds often presents challenges due to the need for specific conditions and reagents, making it a topic of interest for chemists seeking efficient synthetic strategies.
  • Pharmaceutical Relevance: Indole derivatives are often investigated in drug discovery pipelines, highlighting their importance as scaffolds in the development of novel pharmaceuticals.

In the words of a noted chemist, "The allure of the indole structure lies not only in its complexity but in the myriad of possibilities it opens in the realm of bioactive compounds." The ongoing research surrounding compounds like 2,3-dimethyl-1,5,6,7-tetrahydroindol-4-one emphasizes the importance of exploring chemical diversity in the quest for innovative solutions in drug design and therapeutic applications.

Synonyms
6116-75-2
INDOL-4(5H)-ONE, 6,7-DIHYDRO-2,3-DIMETHYL-
BRN 0472114
6,7-Dihydro-2,3-dimethyl-indol-4(5H)-one
DTXSID70210053
5-21-07-00455 (Beilstein Handbook Reference)
DTXCID70132544
2,3-dimethyl-1,5,6,7-tetrahydroindol-4-one
2,3-Dimethyl-1,5,6,7-tetrahydro-4H-indol-4-one
SCHEMBL934852
UORPHFZBCZEBJV-UHFFFAOYSA-N
AKOS000320294
2,3-dimethyl-6,7-dihydro-1H-indole-4(5H)-on