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Thiomesityl

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Identification
Molecular formula
C8H10S
CAS number
100-68-5
IUPAC name
methylsulfanylmethylbenzene
State
State

At room temperature, methylsulfanylmethylbenzene is in a liquid state. It has moderate volatility and can be handled with standard laboratory precautions.

Melting point (Celsius)
-21.00
Melting point (Kelvin)
252.15
Boiling point (Celsius)
216.00
Boiling point (Kelvin)
489.15
General information
Molecular weight
122.21g/mol
Molar mass
122.2060g/mol
Density
1.0540g/cm3
Appearence

Methylsulfanylmethylbenzene is typically a colorless liquid. It may have a faint, characteristic aromatic odor due to the presence of the phenyl group in its structure.

Comment on solubility

Solubility of Methylsulfanylmethylbenzene

Methylsulfanylmethylbenzene, also known as p-Tolyl methyl sulfide, exhibits unique solubility characteristics worth discussing. This compound is largely *organic in nature*, which influences its behavior in various solvents. Here are some key points regarding its solubility:

  • Solvent Polarity: Methylsulfanylmethylbenzene is expected to be *soluble in organic solvents* due to its hydrophobic characteristics.
  • Solubility in Water: It is likely to be *insoluble or only sparingly soluble in water* because of its non-polar structure, which does not interact favorably with polar water molecules.
  • Common Organic Solvents: It typically dissolves well in solvents such as:
    • Ethyl acetate
    • Hexane
    • Chloroform
  • Temperature Effect: Like many organic compounds, solubility may increase with temperature, thus affecting its behavior in different environments.

In conclusion, the solubility of methylsulfanylmethylbenzene reflects its organic nature, being notably soluble in non-polar solvents while exhibiting minimal solubility in polar solvents like water. This property makes it an interesting compound for applications in organic chemistry.

Interesting facts

Interesting Facts about Methylsulfanylmethylbenzene

Methylsulfanylmethylbenzene, commonly known as methyl thioanisole, is a fascinating compound within the arena of organic chemistry. This compound features a unique combination of a methyl group, a sulfur atom, and a benzene ring, resulting in distinct chemical properties and applications.

Key Features

  • Scent: Methylsulfanylmethylbenzene is known for its distinctive and pleasant aroma, reminiscent of a sweet, medicinal odor, which is utilized in fragrance applications.
  • Natural Occurrences: This compound can be found in certain essential oils and is produced by some plants, contributing to their characteristic smells.
  • Reactivity: The presence of the sulfur atom imparts unique reactivity to methylsulfanylmethylbenzene, allowing it to undergo various chemical reactions, such as electrophilic substitution.
  • Applications: Beyond its aromatic properties, this compound is instrumental in the synthesis of various pharmaceuticals, agrochemicals, and other valuable organic compounds.

Scientific Insights

From a molecular perspective, methylsulfanylmethylbenzene exemplifies the influence of functional groups on the overall behavior of compounds. The sulfur atom enhances the stability of the molecule through intramolecular interactions, fostering a robust scaffold for further modifications. According to renowned chemist Linus Pauling, "Chemical bonds are the threads of chemical structure," and in the case of methylsulfanylmethylbenzene, the unique C–S bond plays a fundamental role in determining its properties and potential use cases.

Whether you're exploring its role in organic synthesis or its contributions to the fragrance industry, methylsulfanylmethylbenzene showcases the intricate interplay of chemistry, biology, and industry, making it a compound worthy of study and admiration.

Synonyms
Benzyl methyl sulfide
766-92-7
Methyl benzyl sulfide
Benzyl methyl sulphide
Sulfide, benzyl methyl
1-Phenyl-2-thiapropane
Benzene, [(methylthio)methyl]-
alpha-(Methylthio)toluene
[(Methylsulfanyl)methyl]benzene
((METHYLTHIO)METHYL)BENZENE
FEMA No. 3597
Benzene, ((methylthio)methyl)-
.alpha.-(Methylthio)toluene
Methylthiomethylbenzene
NSC 75125
EINECS 212-174-7
Benzylmethylsulphide
UNII-Y3900RBK51
Y3900RBK51
NSC-75125
methylsulfanyl-methyl-benzene
((methylthio)methyl)-Benzene
[(methylthio)methyl]-Benzene
Sulfide, benzyl methyl (8CI)
DTXSID1061106
FEMA 3597
[(Methylthio)methyl]benzene, 9CI
BENZYL METHYL SULFIDE [FHFI]
BENZYL METHYL SULFIDE [USP-RS]
((Methylsulfanyl)methyl)benzene
((Methylsulphanyl)methyl)benzene
[(Methylsulphanyl)methyl]benzene
((Methylthio)methyl)benzene, 9ci
BENZYL METHYL SULFIDE (USP-RS)
1Phenyl2thiapropane
alpha(Methylthio)toluene
Benzene, ((methylthio)methyl)
DTXCID0047905
inchi=1/c8h10s/c1-9-7-8-5-3-2-4-6-8/h2-6h,7h2,1h
ofqpkkgmnwaspn-uhfffaoysa-n
Benzyl(methyl)sulfane
methylsulfanylmethylbenzene
Benzyl metyl sulfide
MFCD00008563
methylsulanylmethylbenzene
SCHEMBL87756
phenylmethylsulfonium methylide
SCHEMBL2683249
CHEBI:192308
[(Methylsulfanyl)methyl]benzene #
NSC75125
AKOS015899702
AS-81520
PTF
DB-229966
B0992
CS-0322476
NS00022767
D88728
Q27294208