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Dibenzyl sulfoxide

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Identification
Molecular formula
C14H14OS
CAS number
937-30-4
IUPAC name
benzylsulfinylmethylbenzene
State
State

At room temperature, dibenzyl sulfoxide is typically in the solid state. It is a stable compound under standard conditions but may be sensitive to air and light.

Melting point (Celsius)
78.00
Melting point (Kelvin)
351.15
Boiling point (Celsius)
337.00
Boiling point (Kelvin)
610.15
General information
Molecular weight
214.33g/mol
Molar mass
214.2870g/mol
Density
1.1229g/cm3
Appearence

Dibenzyl sulfoxide appears as a white crystalline solid. It is generally odorless and has a distinct crystalline structure that can reflect light, giving it a characteristic sheen.

Comment on solubility

Solubility of Benzylsulfinylmethylbenzene

Benzylsulfinylmethylbenzene, with its unique structure, presents interesting solubility characteristics that are important for various applications. Understanding its solubility can help in determining suitable solvents and conditions for its use. Below are key points regarding its solubility:

  • Polarity: The presence of the sulfinyl group influences the polarity of the compound, which can affect solubility in polar versus non-polar solvents.
  • Solvent Compatibility: This compound tends to be more soluble in organic solvents such as:
    • Ether
    • Toluene
    • Dichloromethane
  • Water Solubility: Benzylsulfinylmethylbenzene is generally expected to have low solubility in water due to its hydrophobic hydrocarbon framework.
  • Temperature Effects: Solubility might increase with temperature; thus, heating the solvent can enhance dissolution.

In summary, while benzylsulfinylmethylbenzene may have limited water solubility, its compatibility with a range of organic solvents makes it versatile for various chemical processes. As always, conducting empirical solubility tests is recommended to obtain precise data for specific applications.

Interesting facts

Interesting Facts about Benzylsulfinylmethylbenzene

Benzylsulfinylmethylbenzene is a fascinating compound that belongs to the class of organic sulfur compounds. It offers a variety of applications and unique characteristics that capture the attention of chemists.

Key Highlights:

  • Structural Complexity: The presence of both benzyl and sulfinyl groups in its structure makes benzylsulfinylmethylbenzene an excellent example of how functional groups can influence chemical properties and reactivity.
  • Potential Applications: This compound may find application in pharmaceuticals, where sulfinyl compounds are often investigated for their medicinal properties. Their potential as prodrugs or active pharmaceutical ingredients can be significant.
  • Reactivity: Sulfinyl compounds like benzylsulfinylmethylbenzene can participate in various chemical reactions, including oxidation and nucleophilic substitutions, making them interesting subjects for organic synthesis.
  • Research Value: Due to its unique structure, it could serve as a valuable intermediate in organic synthesis, contributing to the development of new materials or biological active molecules.

Moreover, this compound can spark discussions about the role of sulfur in organic chemistry and the intriguing chemistry of sulfoxides. As scientific research delves deeper into the functionalities of these compounds, benzylsulfinylmethylbenzene undoubtedly stands out as a compound worth exploring further.

In the words of a chemist, "The exploration of sulfur compounds often leads us to unexpected pathways and novel reactions that challenge our understanding of organic chemistry."


Synonyms
Dibenzyl sulfoxide
Benzyl sulfoxide
Dibenzyl sulphoxide
Benzene, 1,1'-[sulfinylbis(methylene)]bis-
Benzyl sulphoxide
EINECS 210-668-7
Preventol CI 5
BRN 2049262
NSC-55
UNII-554PDF1275
BENZENE, 1,1'-(SULFINYLBIS(METHYLENE))BIS-
AI3-62190
SULFOXIDE,DIBENZYL
554PDF1275
1,1'-[sulfinylbis(methylene)]dibenzene
DTXSID8022088
4-06-00-02651 (Beilstein Handbook Reference)
1,1'-(SULFINYLBIS(METHYLENE))BIS(BENZENE)
1,1'-(sulfinylbis(methylene))dibenzene
DTXCID802088
htmqzwfstjvjeq-uhfffaoysa-n
inchi=1/c14h14os/c15-16(11-13-7-3-1-4-8-13)12-14-9-5-2-6-10-14/h1-10h,11-12h
621-08-9
Dibenzylsulfoxide
Tardiol D
(Sulfinylbis(methylene))dibenzene
Sulfoxide, dibenzyl
benzylsulfinylmethylbenzene
Bis(phenylmethyl) sulfoxide
NSC 55
Dibenzylsulphoxide
MFCD00004782
MLS002637483
CHEMBL190496
Dibenzylsulfoxyd
(phenylmethanesulfinylmethyl)benzene
1,1'-(sulfinyldimethanediyl)dibenzene
benzylsulfinyl-methyl-benzene
NSC55
WLN: R1SO&1R
SCHEMBL340372
sulfinylbis(methylene)dibenzene
[(Benzylsulfinyl)methyl]benzene
BDBM22781
(phenylmethyl)sulfinylmethylbenzene
[(Benzylsulfinyl)methyl]benzene #
[(phenylmethane)sulfinylmethyl]benzene
AKOS004907768
FB01395
Benzene,1'-[sulfinylbis(methylene)]bis-
NCGC00246832-01
AC-16487
AS-61321
SMR001547021
SY050947
1,1'-[sulfinylbis(methylene)]bis-benzene
CS-0204274
D0001
NS00020009
D95355
A833587
AE-641/05560032
Q5805477
Z316995896