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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
State
State

At room temperature, 2-phenyl-1,3-dithiane is in a solid state, usually forming white crystalline structures. It maintains its stability and solid form under standard laboratory conditions.

Melting point (Celsius)
45.00
Melting point (Kelvin)
318.15
Boiling point (Celsius)
281.00
Boiling point (Kelvin)
554.15
General information
Molecular weight
182.30g/mol
Molar mass
182.3000g/mol
Density
1.1875g/cm3
Appearence

2-Phenyl-1,3-dithiane appears as a white solid with a characteristic odor. Its pure form is typically crystalline, and it is often used in its solid state for various chemical synthesis applications.

Comment on solubility

Solubility of 2-phenyl-1,3-dithiane

2-phenyl-1,3-dithiane, with the chemical formula C8H8S2, exhibits particular solubility characteristics that are noteworthy for chemical applications. The solubility of this compound can be understood in the context of its structural features and polarity:

  • Non-polar Nature: Due to its symmetrical structure and the presence of two sulfur atoms, 2-phenyl-1,3-dithiane tends to be relatively non-polar.
  • Solvent Compatibility: This compound is expected to be soluble in non-polar organic solvents such as:
    • Hexane
    • Toluene
    • Chloroform
  • Limited Water Solubility: Conversely, the solubility in water is likely very low, as water is a polar solvent and non-polar molecules do not dissolve well in polar media.
  • Application Implications: Such solubility characteristics make 2-phenyl-1,3-dithiane useful in organic synthesis, where non-polar solvents are preferred.

In conclusion, the solubility profile of 2-phenyl-1,3-dithiane illustrates key principles of solubility rules — "like dissolves like". Understanding these properties is crucial for effective handling and utilization in various chemical processes.

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.

Synonyms
2-Phenyl-1,3-dithiane
1,3-Dithiane, 2-phenyl-
m-DITHIANE, 2-PHENYL-
2-Phenyl-m-dithiane
EINECS 226-568-1
NSC 12763
BRN 0130879
53TCS8B01P
NSC-12763
UNII-53TCS8B01P
DTXSID60202604
5-19-01-00462 (Beilstein Handbook Reference)
2-PHENYL-1,3-DITHIACYCLOHEXANE
DTXCID50125095
1,3-Dithiane, 2-phenyl-(9CI)
226-568-1
gxkpardrbfuron-uhfffaoysa-n
inchi=1/c10h12s2/c1-2-5-9(6-3-1)10-11-7-4-8-12-10/h1-3,5-6,10h,4,7-8h
5425-44-5
2-phenyl-[1,3]dithiane
MFCD00006656
C10H12S2
NSC12763
phenyl-1,3-dithian
2-phenyl-1,3-dithian
2-phenyl-1, 3-dithiane
SCHEMBL24705
2-Phenyl-[1,3]-dithiane
2-Phenyl-1,3-dithiane, 97%
AKOS024319038
CS-W015694
AS-57478
SY235181
DB-021487
NS00043700
P2660
10.14272/GXKPARDRBFURON-UHFFFAOYSA-N
D71190
doi:10.14272/GXKPARDRBFURON-UHFFFAOYSA-N