1-methyl-4-(p-tolylsulfinyl)benzene

Identification

Molecular formula

C₁₄H₁₄OS

CAS number

4775-80-8

IUPAC name

1-methyl-4-(p-tolylsulfinyl)benzene

State

At room temperature, the compound is typically a solid.

Melting point (Celsius)

85.00

Melting point (Kelvin)

358.15

Boiling point (Celsius)

380.00

Boiling point (Kelvin)

653.15

General information

Molecular weight

230.32g/mol

Molar mass

230.3200g/mol

Density

1.2300g/cm³

Appearence

1-methyl-4-(p-tolylsulfinyl)benzene appears as a white solid in its pure form. It can form crystalline structures under appropriate conditions.

Comment on solubility

Solubility of 1-methyl-4-(p-tolylsulfinyl)benzene

1-methyl-4-(p-tolylsulfinyl)benzene, a compound characterized by its complex aromatic structure, displays interesting solubility properties influenced by the presence of the sulfinyl group. Understanding its solubility can offer insights into its behavior in various environments:

Non-polar Solvents: This compound is expected to have enhanced solubility in non-polar solvents, owing to its predominantly hydrophobic character arising from the benzene rings and methyl substituents.
Polar Solvents: Solubility in polar solvents, like water, is likely to be limited due to the lack of ionic or highly polar functional groups that would interact favorably with water molecules.
Temperature Effect: As with many organic compounds, an increase in temperature can increase solubility, allowing for better dissolution in non-polar media.
Hydrophobic Interactions: The hydrophobic nature of the aromatic rings makes this compound less miscible with polar solvents, highlighting the importance of considering solvent polarity in solubility evaluations.

In summary, the solubility of 1-methyl-4-(p-tolylsulfinyl)benzene is intricately linked to its structural characteristics and the nature of the solvent. Such insights are crucial for applications in synthesis and the development of materials where solubility plays a key role.

Interesting facts

Interesting Facts about 1-Methyl-4-(p-tolylsulfinyl)benzene

1-Methyl-4-(p-tolylsulfinyl)benzene, commonly referred to in the scientific community as a *sulfinyl-containing aromatic compound*, showcases a unique blend of structural characteristics that contribute to its diverse applications in organic chemistry.

Unique Structural Features

Functional Groups: The presence of a sulfinyl group offers intriguing reactivity, making this compound a valuable candidate for various chemical transformations.
Substituent Effects: The methyl and p-tolyl groups can influence the electronic properties, enhancing its role in electrophilic aromatic substitution reactions.

Applications in Chemistry

This compound serves as a key intermediate in synthetic organic chemistry, participating in the development of:

Pharmaceuticals: Its sulfinyl moiety is often found in drugs, contributing to biological activity.
Agricultural Chemicals: Sulfinyl derivatives can exhibit herbicidal properties, showcasing their utility beyond medicinal applications.

Notable Reactions

In the realm of organic synthesis, 1-methyl-4-(p-tolylsulfinyl)benzene can engage in:

Nucleophilic Substitution: The sulfinyl group can act as a leaving group, allowing for the introduction of various nucleophiles.
Oxidation Processes: It can oxidatively transform into sulfone derivatives, expanding its functional group repertoire.

This compound acts as a prime example of how small modifications in molecular structure can lead to dramatic changes in reactivity and application. As you explore the depth of organic chemistry, remember that compounds like 1-methyl-4-(p-tolylsulfinyl)benzene exemplify the beauty of synthetic versatility and functional diversity.

Synonyms

p-Tolyl sulfoxide

Diptolyl sulfoxide

Bis(ptolyl)sulphoxide

4,4'Ditolyl sulfoxide

p-Tolyl sulfoxide (8CI)

Toluene, 4,4'sulfinylbis

pToluene, 1,1'sulfinylbis

Benzene, 1,1'sulfinylbis(4methyl

Benzene, 1,1'sulfinylbis(4methyl (9CI)

1774-35-2

Di-p-tolyl sulfoxide

Benzene, 1,1'-sulfinylbis[4-methyl-

Ditolyl sulfoxide

4,4'-Sulfinylbis(methylbenzene)

Sulfoxide, ditolyl

Ditolyl sulphoxide

1-methyl-4-(4-methylphenyl)sulfinylbenzene

4,4'-Ditolyl sulfoxide

Toluene, 4,4'-sulfinylbis-

1-methyl-4-(4-methylbenzenesulfinyl)benzene

NSC 73128

p-TOLUENE, 1,1'-SULFINYLBIS-

Benzene, 1,1'-sulfinylbis(4-methyl-

4,4/'-Dimethyldiphenylsulfoxide

4,4'-Dimethyldiphenylsulfoxide

Bis(p-tolyl)sulphoxide

EINECS 217-203-7

BRN 2048587

bis(4-methylphenyl) sulfoxide

p-tolylsulfoxide

MFCD00008546

Toluene,4'-sulfinylbis-

p-Tolyl sulfoxide, 97%

Benzene, 1,1'-sulfinylbis(4-methyl- (9CI)

p-Toluene,1'-sulfinylbis-

bis(4-methylphenyl)sulfoxide

NCIOpen2_003744

4,4-Dimethyldiphenylsulfoxide

4-06-00-02173 (Beilstein Handbook Reference)

Bis(p-methylphenyl) sulfoxide

MLS000105795

SCHEMBL235851

WLN: 1R DSO&R D1

CHEMBL1366230

MJWNJEJCQHNDNM-UHFFFAOYSA-

DTXSID40170296

Benzene,1'-sulfinylbis[4-methyl-

HMS2406I07

NSC73128

NSC-73128

AKOS005167035

AC-4577

AS-62176

SMR000102772

DB-080923

NS00025851

T1075

4-methyl-1-[(4-methylphenyl)sulfinyl]benzene

Benzene,1-methyl-4((phenylmethyl)sulfinyl))-

D92446

1-Methyl-4-[(4-methylphenyl)sulfinyl]benzene #

InChI=1/C14H14OS/c1-11-3-7-13(8-4-11)16(15)14-9-5-12(2)6-10-14/h3-10H,1-2H3