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2-Methyl-2-phenyl-1,3-dithiane

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Identification
Molecular formula
C10H12S2
CAS number
7383-51-1
IUPAC name
2-methyl-2-phenyl-1,3-dithiane
State
State

At room temperature, 2-Methyl-2-phenyl-1,3-dithiane is a solid compound, typically stable under standard laboratory conditions.

Melting point (Celsius)
74.00
Melting point (Kelvin)
347.00
Boiling point (Celsius)
318.00
Boiling point (Kelvin)
591.00
General information
Molecular weight
208.35g/mol
Molar mass
208.3500g/mol
Density
1.1900g/cm3
Appearence

2-Methyl-2-phenyl-1,3-dithiane typically appears as a slightly yellowish crystalline solid, with a faint aromatic odor. It crystallizes into well-defined structures.

Comment on solubility

Solubility of 2-methyl-2-phenyl-1,3-dithiane

The solubility of 2-methyl-2-phenyl-1,3-dithiane in different solvents is an intriguing aspect to consider. This compound, characterized by the presence of dithiane rings, reflects unique solubility properties due to its molecular structure.

  • Polar Solvents: It is less soluble in highly polar solvents like water due to the hydrophobic characteristics imparted by its hydrocarbon substituents.
  • Non-Polar Solvents: Conversely, 2-methyl-2-phenyl-1,3-dithiane finds better solubility in non-polar solvents such as hexane or benzene, aligning with the general principle that "like dissolves like."
  • Solvent Interactions: Interaction with solvents can also play a significant role; for instance, the larger phenyl group may hinder interactions with polar molecules.

To summarize, the solubility of 2-methyl-2-phenyl-1,3-dithiane can be categorized as follows:

  1. Insoluble in water and other polar solvents.
  2. Soluble in non-polar solvents such as hexane and benzene.

Understanding such solubility dynamics is essential for applications in chemistry, where solvent selection can vastly influence reactions and product formation.

Interesting facts

Interesting Facts About 2-Methyl-2-phenyl-1,3-dithiane

2-Methyl-2-phenyl-1,3-dithiane is a fascinating compound that belongs to the class of organic sulfur compounds. Its unique structure and properties make it an interesting subject of study in organic chemistry. Here are some key facts:

  • Structural Unique Features: The compound contains two sulfur atoms within a six-membered ring along with a methyl group and a phenyl group attached to the same carbon. This arrangement contributes to its interesting reactivity and stability.
  • Functional Versatility: 2-Methyl-2-phenyl-1,3-dithiane is known for its role as a versatile building block in organic synthesis, particularly in the formation of various carbon-carbon bonds.
  • Synthesis Pathways: One notable synthesis route involves the reaction of thioketones with organolithium reagents, showcasing the utility of this compound in synthesizing more complex organic molecules.
  • Applications in Organic Chemistry: The compound is often used in the synthesis of other important organic compounds, emphasizing its contribution to diverse fields such as pharmaceuticals and specialty chemicals.
  • Research Interest: Since the mid-20th century, 2-methyl-2-phenyl-1,3-dithiane has attracted interest due to its intriguing reactivity patterns, offering insights into sulfur chemistry and its applications in catalytic processes.
  • Potential Benefits: Compounds like 2-methyl-2-phenyl-1,3-dithiane can offer benefits in the development of agrochemicals and materials science, showcasing the broad applicability of sulfur-containing compounds in modern chemistry.

In summary, 2-methyl-2-phenyl-1,3-dithiane not only deepens our understanding of sulfur chemistry but also serves as a valuable precursor in the synthesis of various organic compounds. Its continuous exploration highlights the complex nature of organic reactions and the creative possibilities that arise from unconventional building blocks.

Synonyms
2-Methyl-2-phenyl-m-dithiane
1,3-Dithiane, 2-methyl-2-phenyl-
m-DITHIANE, 2-METHYL-2-PHENYL-
2-Methyl-2-phenyl-1,3-dithiane
DKE4TIO6XH
6331-22-2
NSC 47056
UNII-DKE4TIO6XH
Acetophenone trimethylene dithioketal
NSC-47056
Acetophenone, cyclic trimethylene mercaptole
DTXSID30212699
DTXCID10135190
cavoribxcdtnbo-uhfffaoysa-n
CMLDBU00003567
NSC47056
SCHEMBL8064830