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3,3'-Diethylthiacyanine

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Identification
Molecular formula
C25H26N2S2
CAS number
3326-32-7
IUPAC name
3-ethyl-2-[3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)-2-methyl-prop-2-enylidene]-1,3-benzothiazole
State
State

3,3'-Diethylthiacyanine is typically a solid at room temperature.

Melting point (Celsius)
312.00
Melting point (Kelvin)
585.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
410.62g/mol
Molar mass
410.5810g/mol
Density
1.2650g/cm3
Appearence

3,3'-Diethylthiacyanine appears as an odorless black powder.

Comment on solubility

Solubility of 3-ethyl-2-[3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)-2-methyl-prop-2-enylidene]-1,3-benzothiazole

The solubility of the compound 3-ethyl-2-[3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)-2-methyl-prop-2-enylidene]-1,3-benzothiazole can be influenced by several factors:

  • Polarity: As a derivative of benzothiazole, the compound likely exhibits moderate polarity, potentially affecting its solubility in water and organic solvents.
  • Functional Groups: The presence of functional groups such as the ethyl and methylene components may enhance solubility in nonpolar solvents. Conversely, the ionic characteristics of the benzothiazolium component could promote solubility in polar solvents.
  • Solvent Interaction: The compound is expected to be more soluble in organic solvents like methanol or ethanol, due to its molecular structure, while demonstrating lower solubility in water.

In general, solubility is a critical property that determines the behavior of a compound in various environments. As John Dalton famously stated, "Solubility is the first place where the magic happens!" Thus, understanding the solubility of this compound provides insights into its potential applications and reactivity in different media.

Interesting facts

Interesting Facts about 3-ethyl-2-[3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)-2-methyl-prop-2-enylidene]-1,3-benzothiazole

This compound, a fascinating organic molecule, belongs to the family of benzothiazole derivatives. These compounds have garnered attention in various fields such as medicinal chemistry and materials science due to their unique properties and versatile applications.

Unique Structural Features

  • Complex framework: The structure comprises a benzothiazole core, which is known for its *heterocyclic nature* and contributes to the molecule's reactivity and stability.
  • Functional versatility: The presence of ethyl and prop-2-enylidene groups enables a diverse range of chemical transformations, making the compound a subject of interest for synthetic chemists.
  • Ionizable nitrogen: The inclusion of a positively charged nitrogen in the benzothiazolium moiety highlights the molecule's potential for interesting interactions in ionic solutions.

Applications and Importance

3-ethyl-2-[3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)-2-methyl-prop-2-enylidene]-1,3-benzothiazole shows promise in several areas:

  • Antibacterial activity: Compounds like these often exhibit significant antibacterial properties, making them candidates for developing new medicinal agents.
  • Photovoltaic applications: The unique properties of benzothiazole derivatives may enhance the efficiency of organic solar cells, contributing to the ever-evolving field of renewable energy.
  • Dyes and pigments: The vibrant colors originating from benzothiazole structures are utilized in dyes, suggesting potential uses in textiles and inks.

Research and Future Directions

Ongoing research aims to optimize the synthesis and explore the biological potential of this compound. Scientists are investigating:

  • Targeted drug delivery: The compound's structure could be modified to facilitate specific targeting of cells, enhancing therapeutic efficacy.
  • Environmental applications: Utilizing its properties for environmental remediation may pave the way for detoxifying pollutants.

As a compound rich in potential, 3-ethyl-2-[3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)-2-methyl-prop-2-enylidene]-1,3-benzothiazole exemplifies the beauty and complexity of chemical exploration, encouraging scientists to delve deeper into its myriad applications.

Synonyms
SCHEMBL2409472