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2,3-Dimethylindoline

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Identification
Molecular formula
C10H13N
CAS number
6057-19-2
IUPAC name
2,3-dimethylindoline
State
State

At room temperature, 2,3-Dimethylindoline is a liquid. It should be kept sealed under inert gas to prevent oxidation, as exposure to air may cause it to oxidize or degrade.

Melting point (Celsius)
-3.00
Melting point (Kelvin)
270.15
Boiling point (Celsius)
238.00
Boiling point (Kelvin)
511.15
General information
Molecular weight
147.22g/mol
Molar mass
147.2230g/mol
Density
1.0090g/cm3
Appearence

2,3-Dimethylindoline is typically a colorless to pale yellow liquid. It is an aromatic compound, and under prolonged exposure to air or light, it may darken. This compound should be stored in a cool, dry place, and handled with appropriate safety precautions due to its chemical nature.

Comment on solubility

Solubility of 2,3-dimethylindoline

2,3-dimethylindoline, with its unique structure, presents interesting solubility characteristics that are worth noting. Overall, its solubility profile can be influenced by various factors:

  • Polarity: The presence of methyl groups on the indoline structure typically increases its non-polar character, leading to lower solubility in polar solvents like water.
  • Solvent Compatibility: It is generally more soluble in non-polar organic solvents such as hexane or dichloromethane, making it suitable for applications in organic synthesis.
  • Temperature Effect: As is common with organic compounds, temperature can significantly affect solubility; warming the solvent often enhances the solubility of 2,3-dimethylindoline.

To summarize, while 2,3-dimethylindoline exhibits limited solubility in polar environments, its enhanced compatibility with non-polar solvents allows it to be utilized effectively in various chemical processes. Understanding these solubility dynamics is essential for chemists working with this compound.

Interesting facts

Interesting Facts About 2,3-Dimethylindoline

2,3-Dimethylindoline is a fascinating organic compound that belongs to the indoline family, which is characterized by its unique bicyclic structure. Here are some intriguing aspects of this compound:

  • Structural Diversity: The presence of two methyl groups at the 2 and 3 positions of the indoline ring system introduces structural diversity that can influence the compound's reactivity and properties. This structural modification can lead to variations in biological activity and functional applications.
  • Application in Organic Synthesis: 2,3-Dimethylindoline serves as an important intermediate in organic synthesis. Its versatility allows it to be transformed into various derivatives, which are often utilized in the development of pharmaceuticals, agrochemicals, and other fine chemicals.
  • Potential in Drug Development: Compounds related to indolines, including 2,3-dimethylindoline, have been researched for their potential biological activities, including anti-cancer and anti-inflammatory properties. Studies continue to explore the therapeutic applications of indoline derivatives in modern medicine.
  • Chemical Reactivity: 2,3-Dimethylindoline exhibits interesting chemical reactivity due to the presence of nitrogen in the bicyclic structure, which can participate in various reactions such as electrophilic substitution and condensation reactions.
  • Research and Studies: The compound has attracted attention in several research domains, inspiring numerous studies aimed at uncovering its properties, mechanisms of action, and potential applications. Scholars often cite this compound when discussing the properties of nitrogen-containing heterocycles.

In summary, 2,3-dimethylindoline is not just a simple organic molecule; it represents a gateway to understanding more complex chemical phenomena and applications in various fields of science. Its structural intricacies and reactivity patterns make it an excellent subject for both academic study and practical applications in chemistry.

Synonyms
2,3-Dimethylindoline
2,3-dimethyl-2,3-dihydro-1H-indole
DTXSID60908033
RefChem:442475
DTXCID101337120
103-638-9
22120-50-9
MFCD00005707
PE-12
10276-90-1
1H-Indole, 2,3-dihydro-2,3-dimethyl-
2,3-Dimethyl-2,3-dihydroindole
BRN 0122361
INDOLINE, 2,3-DIMETHYL-
5-20-06-00396 (Beilstein Handbook Reference)
SCHEMBL172934
SCHEMBL6865922
SCHEMBL29501187
NNPSOAOENINXMR-UHFFFAOYSA-N
NSC62098
XAA12050
NSC-62098
AKOS006282822
DS-4336
SB64043
SY105392
DB-045801
CS-0137235
C74121
EN300-6472873
F242103