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2-Ethylsulfonylbenzothiazole

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Identification
Molecular formula
C9H9NO2S2
CAS number
5726-52-1
IUPAC name
2-ethylsulfonyl-1,3-benzothiazole
State
State

At room temperature, 2-ethylsulfonylbenzothiazole is typically solid. It has a high melting point that keeps it in solid state under normal conditions.

Melting point (Celsius)
73.00
Melting point (Kelvin)
346.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
213.30g/mol
Molar mass
213.2900g/mol
Density
1.4500g/cm3
Appearence

2-Ethylsulfonylbenzothiazole is typically a crystalline solid. Its appearance can vary, but it is generally found as a white to off-white solid.

Comment on solubility

Solubility of 2-Ethylsulfonyl-1,3-benzothiazole

2-Ethylsulfonyl-1,3-benzothiazole exhibits interesting solubility characteristics that depend largely on the solvent used. Generally speaking, the solubility of this compound can be influenced by key factors such as:

  • Polarity: Being a sulfonyl compound, it tends to have moderate solubility in polar solvents like water and alcohols.
  • Hydrophobicity: The aromatic benzothiazole ring confers some hydrophobic properties, which may limit solubility in very polar environments.
  • Temperature: As with many compounds, solubility often increases with temperature, making it more soluble in hot solvents than in cold ones.

Quantitative assessments indicate that the solubility may be categorized as follows:

  1. High solubility: Common organic solvents like dimethyl sulfoxide (DMSO) and acetone.
  2. Moderate solubility: Examples include methanol and ethyl acetate.
  3. Low solubility: Some more nonpolar solvents may not effectively solvate this compound.

In summary, the solubility of 2-ethylsulfonyl-1,3-benzothiazole varies significantly depending on the choice of solvent, illustrating its unique chemical structure and interactions. As noted, "the environment greatly influences solubility," making it essential to consider solvent properties in any application involving this compound.

Interesting facts

Interesting Facts about 2-Ethylsulfonyl-1,3-benzothiazole

2-Ethylsulfonyl-1,3-benzothiazole is a fascinating compound that presents a unique blend of properties and applications, making it noteworthy in the field of chemical sciences. Here are some interesting aspects to consider:

  • Versatile Structural Features: This compound is characterized by the presence of both a sulfonyl group and a benzothiazole ring, which contribute to its chemical reactivity and possible interactions with biological molecules.
  • Applications in Agriculture: Compounds similar to 2-ethylsulfonyl-1,3-benzothiazole have been studied for their potential use as fungicides and herbicides, providing insights into protecting crops against various pathogens.
  • Role in Pharmaceuticals: The benzothiazole moiety is known for its presence in many medicinal compounds, offering a pathway for drug development targeting diseases, notably in the fields of oncology and infectious diseases.
  • Investigation of Physical Properties: Researchers often delve into the compound's unique interactions and behaviors under different conditions, which can impact their practical uses.
  • Environmental Considerations: As with many chemical compounds, studying the environmental impact and degradation of 2-ethylsulfonyl-1,3-benzothiazole is crucial for sustainable use.

In summary, 2-ethylsulfonyl-1,3-benzothiazole is not just a simple compound; it stands at the intersection of agriculture, pharmaceuticals, and environmental science. Its multifaceted nature invites further research and discussion among scientists and students alike.

Synonyms
2591-11-9
BENZOTHIAZOLE, ETHYLSULFONYL-
2-(ethylsulfonyl)benzothiazole
Ethylsulfonylbenzothiazole
Ethyl 2-benzothiazyl sulfone
benzothiazole, 2-(ethylsulfonyl)-
SCHEMBL3595617
DTXSID00180578
2-(ethylsulfonyl)benzo[d]thiazole
ZYGPCLHWVYJMPA-UHFFFAOYSA-N
2-(ethylsulfonyl)-1,3-benzothiazole
2-(Ethanesulfonyl)-1,3-benzothiazole
AKOS024342784
2-(ethyl sulfonyl)-1,3-benzothiazole
InChI=1/C9H9NO2S2/c1-2-14(11,12)9-10-7-5-3-4-6-8(7)13-9/h3-6H,2H2,1H