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2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde

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Identification
Molecular formula
C14H15NO
CAS number
16265-28-8
IUPAC name
2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde
State
State

At room temperature, 2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde is typically found as a solid. Its relatively high melting point indicates that it remains in a solid state under standard laboratory conditions.

Melting point (Celsius)
108.00
Melting point (Kelvin)
381.15
Boiling point (Celsius)
300.50
Boiling point (Kelvin)
573.65
General information
Molecular weight
213.28g/mol
Molar mass
213.2840g/mol
Density
1.0700g/cm3
Appearence

2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde typically appears as a yellow to dark orange crystalline solid. The compound's color can vary depending on its purity and the specific conditions under which it is stored or observed.

Comment on solubility

Solubility of 2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde

The solubility of 2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde is influenced by its molecular structure and composition. This compound is a complex organic compound, and its solubility can be described in various contexts:

  • Polar vs. Non-polar Solvents: As a generally non-polar compound, 2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde tends to have limited solubility in polar solvents such as water. However, it is likely to be more soluble in non-polar organic solvents such as hexane, ether, or benzene.
  • Temperature Dependency: The solubility of organic compounds often increases with temperature. Therefore, heating the solvent might enhance the solubility of this compound.
  • Functional Groups: The presence of the aldehyde functional group (–CHO) may introduce some degree of reactivity and interactions with other molecules, potentially affecting solubility in various media.

In summary, the solubility of 2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde is not straightforward and varies based on the solvent used. Remember, "Like dissolves like" is a guiding principle; hence one should choose the solvent carefully.

Interesting facts

Interesting Facts about 2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde

2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde is a fascinating compound that plays a significant role in various fields of chemistry and materials science. Here are some intriguing aspects:

  • Versatile Application: This compound is notable for its application in organic synthesis, particularly in the development of new pharmaceuticals and agrochemicals. Its unique structure allows for ease of modification, leading to a multitude of derivatives.
  • Involvement in Photocatalysis: Researchers have identified that this compound exhibits interesting photocatalytic properties. This makes it a potential candidate for use in solar energy applications and the development of sustainable chemical processes.
  • Structure-Activity Relationship: The compound’s structure can greatly influence its biological activity. The indoline moiety is known for its biological significance, particularly in medicinal chemistry, where modifications can lead to enhanced efficacy against specific targets.
  • Novel Applications: Beyond organic synthesis, this compound may find applications in the fields of dye-sensitized solar cells (DSSCs) and organic light-emitting diodes (OLEDs) due to its electronic characteristics.

In summary, 2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde is not just a simple organic molecule; it holds great potential in the advancement of science and technology. As a student or researcher, exploring its vast capabilities offers an exciting journey into the world of chemical innovation.

Synonyms
84-83-3
2-(1,3,3-Trimethylindolin-2-ylidene)acetaldehyde
Acetaldehyde, (1,3-dihydro-1,3,3-trimethyl-2H-indol-2-ylidene)-
2-(1,3,3-trimethylindol-2-ylidene)acetaldehyde
DTXSID7052579
1,3-Dihydro-1,3,3-trimethyl-2H-indol-2-ylidene acetaldehyde
(E)-2-(1,3,3-trimethylindolin-2-ylidene)acetaldehyde
85654-15-5
1127303-63-2
MFCD00071813
DTXCID8031152
CHEBI:170032
GCECACVNILMTRD-UHFFFAOYSA-N
AKOS025243272
SB65585
SB65941
1,3,3-trimethyl-2-formylmethyleneindole
SY079216
DB-019353
NS00038682
D70380
2-[(2Z)-1,3,3-trimethylindol-2-ylidene]acetaldehyde
F1034-0113
201-565-8