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3,3'-Diethylthiacyanine iodide

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Identification
Molecular formula
C22H20N2S2
CAS number
314-13-6
IUPAC name
3-ethyl-2-[3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)prop-2-enylidene]-1,3-benzothiazole
State
State

At room temperature, the compound is typically in a solid state, appearing as crystalline powder.

Melting point (Celsius)
233.00
Melting point (Kelvin)
506.15
Boiling point (Celsius)
288.00
Boiling point (Kelvin)
561.15
General information
Molecular weight
490.64g/mol
Molar mass
490.6400g/mol
Density
1.2600g/cm3
Appearence

The compound typically appears as dark red crystals. These crystals are known for their intense color, which is a characteristic of many cyanine dyes.

Comment on solubility

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

The solubility of the compound 3-ethyl-2-[3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)prop-2-enylidene]-1,3-benzothiazole is influenced by several factors that stem from its complex molecular structure. Here are key points regarding its solubility:

  • Polarity: The presence of benzothiazole rings and the cationic nature from the 1,3-benzothiazol-3-ium moiety typically enhances solubility in polar solvents, particularly water.
  • Solvent Interaction: The compound is more likely to dissolve well in polar solvents such as ethanol and methanol due to possible hydrogen bonding and dipole-dipole interactions.
  • Temperature Sensitivity: Like many organic compounds, its solubility may increase with higher temperatures, allowing for more effective molecular interactions.
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In summary, while the solubility of this complex compound may not be extensively documented, it is essential to consider the roles of polarity, solvent choice, and temperature when assessing its solubility characteristics. Careful experimentation may uncover specific solubility behavior relevant to its potential applications.

Interesting facts

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

This fascinating compound is part of the benzothiazole family, which encompasses a variety of biologically significant derivatives. The benzothiazole structure has been widely studied for its involvement in numerous chemical and pharmaceutical applications. Here are some intriguing aspects of this compound:

  • Biological activity: Compounds belonging to the benzothiazole class often exhibit remarkable activities, including antimicrobial, antifungal, and anticancer properties, making them valuable in medicinal chemistry.
  • Synthetic versatility: The presence of ethyl and prop-2-enylidene groups in this compound enhances its synthetic opportunities, enabling the development of derivatives with tailored properties.
  • Electronics and materials: Benzothiazole derivatives are also explored for their potential in organic electronics, especially in designing light-emitting diodes (LEDs) and photovoltaic devices.
  • Fluorescent properties: Compounds in this family often possess fluorescence characteristics, making them useful in various imaging applications and as fluorescent probes.

As the study of complex organic compounds like this one continues to advance, the potential for discovering new applications grows exponentially. The subprocess of exploring these compounds provides insights not only into structural chemistry but also their profound implications in improving health and technology.

Synonyms
3,3'-diethylthiacarbocyanine
YBM8W799TH
Crysta-lyn 551024 cation
18403-49-1
Benzothiazolium, 3-ethyl-2-(3-(3-ethyl-2-benzothiazolinylidene)propenyl)-
Benzothiazolium, 3-ethyl-2-(3-(3-ethyl-2(3H)-benzothiazolylidene)-1-propen-1-yl)-
Benzothiazolium, 3-ethyl-2-(3-(3-ethyl-2(3H)-benzothiazolylidene)-1-propenyl)-
GNF-PF-3148
UNII-YBM8W799TH
DTXSID9048352