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2-Chloro-1,3,2-dithiarsolane

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Identification
Molecular formula
C2H3AsClS2
CAS number
4731-51-7
IUPAC name
2-chloro-1,3,2-dithiarsolane
State
State

At room temperature, it exists as a liquid. Handle with care due to its chemical reactivity and potential toxicity.

Melting point (Celsius)
-35.00
Melting point (Kelvin)
238.15
Boiling point (Celsius)
102.00
Boiling point (Kelvin)
375.15
General information
Molecular weight
192.52g/mol
Molar mass
192.5200g/mol
Density
2.0100g/cm3
Appearence

2-Chloro-1,3,2-dithiarsolane is typically a colorless liquid that can exhibit a slight yellowish hue due to impurities. It is known for its characteristic odor derived from the presence of sulfur and arsenic in the molecular structure.

Comment on solubility

Solubility of 2-chloro-1,3,2-dithiarsolane

2-chloro-1,3,2-dithiarsolane, with its unique chemical structure, exhibits interesting solubility characteristics. Here are some key points to consider:

  • Polarity: The presence of chlorine and sulfur atoms contributes to its polar nature, which can affect its solubility in various solvents.
  • Solvent Compatibility: This compound is generally more soluble in polar organic solvents such as methanol and ethanol, compared to non-polar solvents like hexane.
  • Aqueous Solubility: Due to the presence of sulfur, solubility in water is limited. However, it may have some degree of solubility in alkaline solutions, where it can undergo reactions with hydroxide ions.
  • Temperature Effects: As with many compounds, solubility can increase with temperature, so heating may enhance its dissolution in specific solvents.

Overall, 2-chloro-1,3,2-dithiarsolane demonstrates selective solubility, aligning with its chemical properties. When experimenting with this compound, consider the solvent choice to maximize its utility in chemical processes.

Interesting facts

Interesting Facts about 2-chloro-1,3,2-dithiarsolane

2-chloro-1,3,2-dithiarsolane is a fascinating compound that hails from the category of organosulfur compounds. This distinct molecule displays several intriguing characteristics that showcase the diversity of chemical interactions in organic chemistry.

Key Features:

  • Structural Uniqueness: The compound's structure features a five-membered ring containing not just carbon and chlorine, but also two sulfur atoms and a central highly reactive phosphorus atom. This unusual arrangement bestows the compound with a variety of reactivity patterns.
  • Synthetic Relevance: 2-chloro-1,3,2-dithiarsolane serves as a crucial intermediate in organic synthesis, particularly in the preparation of more complex sulfur-containing molecules. Its versatility makes it a valuable resource for chemists looking to explore new avenues in material science.
  • Biological Implications: Research has indicated that derivatives of dithiarsolane compounds may exhibit interesting biological activities. Some studies have suggested potential applications in pharmacology, where they could play a role in the design of new drugs.
  • Environmental Interest: Organosulfur compounds like 2-chloro-1,3,2-dithiarsolane may also have significance in environmental chemistry, influencing biogeochemical cycles and contributing to our understanding of sulfur-related processes.

Overall, the study of 2-chloro-1,3,2-dithiarsolane not only enriches our knowledge of organosulfur chemistry but also opens doors to innovative research applications in multiple fields. As noted by one chemist, "The beauty of this compound lies in its complexity and potential for discovery." With ongoing research and exploration, who knows what new insights await in the world of dithiarsolane chemistry?

Synonyms
1,3,2-DITHIARSOLANE, 2-CHLORO-
3741-32-0
BRN 0969361
1,3,2-Dithiarsenole, 2-chlorodihydro-
Ethylene chlorothioarsenate(III)
AI3-15006
2-Chloro-4,5-dihydro-1,3,2-dithiarsenole
2-chloro-1,3,2-dithiaarsolane
DTXSID20190851