2-phenyl-1,3-dithiane

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Identification

Molecular formula
C9H10S2
CAS Number
55111-62-7
IUPAC Name
2-phenyl-1,3-dithiane
Molecular Weight
182.30g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1875g/cm3
Synonyms
2-Phenyl-1, 3-dithiane
Interesting facts

Interesting Facts about 2-Phenyl-1,3-dithiane

2-Phenyl-1,3-dithiane is a fascinating organosulfur compound that belongs to a class known as dithianes. This compound has garnered attention in the field of organic chemistry for various reasons:

  • Unique Structure: The structure of 2-phenyl-1,3-dithiane features a five-membered ring containing sulfur atoms. This unique arrangement provides interesting reactivity and stability characteristics.
  • Synthetic Applications: 2-Phenyl-1,3-dithiane is often used as a building block in the synthesis of more complex organic molecules. Its ability to undergo various reactions allows chemists to produce a wide range of derivatives.
  • Reactivity: This compound can react in nucleophilic substitution reactions due to the presence of sulfur atoms, making it useful for functionalizing organic substrates.
  • Role in Organosulfur Chemistry: 2-Phenyl-1,3-dithiane acts as an important intermediate in the study of organosulfur compounds, which are crucial in pharmaceuticals, agrochemicals, and materials science.
  • Interesting Insights: One researcher noted, "The versatility of dithianes such as 2-phenyl-1,3-dithiane exemplifies the endless possibilities in organic synthesis." This emphasizes their significance in chemical research.

In conclusion, 2-phenyl-1,3-dithiane is not just a simple compound but a key player in organic synthesis and reactivity studies. Its contribution to advancing chemical knowledge cannot be understated.

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