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Phenyl 2-chloroethyl sulfone

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Identification
Molecular formula
C8H9ClO2S
CAS number
5535-48-8
IUPAC name
2-chloroethylsulfonylbenzene
State
State

At room temperature, Phenyl 2-chloroethyl sulfone is a solid, specifically characterized by its crystalline form.

Melting point (Celsius)
66.00
Melting point (Kelvin)
339.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
218.68g/mol
Molar mass
218.6770g/mol
Density
1.3658g/cm3
Appearence

Phenyl 2-chloroethyl sulfone is a crystalline solid. It typically appears as white or off-white crystals or powder, offering a reliable indicator of its purity and stability under standard conditions.

Comment on solubility

Solubility of 2-chloroethylsulfonylbenzene

2-chloroethylsulfonylbenzene, with its unique chemical structure, exhibits noteworthy solubility characteristics. Understanding its solubility is essential as it influences its applications in various chemical processes.

Solubility Profile:

  • Solvent Compatibility: This compound is moderately soluble in polar organic solvents such as ethanol and acetone.
  • Water Solubility: It exhibits relatively low solubility in water due to its hydrophobic aromatic structure, which hinders interactions with water molecules.
  • Temperature Impact: As with many organic compounds, solubility tends to increase with temperature, making hot solvents more effective for dissolution.

In summary, while 2-chloroethylsulfonylbenzene can dissolve in certain polar solvents, its limited solubility in water emphasizes the importance of selecting appropriate solvents for its utilization in research and industrial applications. As the saying goes, "Like dissolves like", and this is especially true for this compound in the context of its solubility behavior.

Interesting facts

Interesting Facts about 2-Chloroethylsulfonylbenzene

2-Chloroethylsulfonylbenzene is a fascinating compound with diverse applications in chemistry and industry. This compound is a type of sulfonamide, characterized by its unique structure that combines a chlorinated ethyl group with a benzenesulfonyl moiety. Here are several compelling facts about this compound:

  • Versatile Intermediate: It is widely used as a synthetic intermediate in the production of pharmaceuticals, pesticides, and dyes, showcasing its importance in chemical synthesis.
  • Electrophile Nature: The presence of the sulfonyl group makes it an excellent electrophile, enabling it to readily participate in nucleophilic substitution reactions.
  • Chemical Reactivity: Its chlorinated ethyl group facilitates various chemical transformations, adding to its utility in organic chemistry.
  • Biological Activities: Compounds derived from 2-chloroethylsulfonylbenzene have shown potential biological activities, which may lead to the development of new therapeutic agents.

As a compound with multifaceted applications, 2-chloroethylsulfonylbenzene exemplifies the dynamic nature of organic chemistry. Its functional groups not only enhance its reactivity but also open doors to innovative discoveries. In the words of chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This sentiment perfectly encapsulates the prospects of working with adaptable compounds like 2-chloroethylsulfonylbenzene.

Synonyms
938-09-0
[(2-Chloroethyl)sulfonyl]benzene
((2-Chloroethyl)sulphonyl)benzene
((2-CHLOROETHYL)SULFONYL)BENZENE
[(2-Chloroethyl)sulphonyl]benzene
EINECS 213-337-5
DTXSID60239652
NSC 145234
NSC 207409
NSC 236821
DTXCID10162143
213-337-5
2-Chloroethyl phenyl sulfone
2-Chloroethylsulfonylbenzene
(2-chloroethylsulfonyl)benzene
(2-chloroethanesulfonyl)benzene
Sulfone, 2-chloroethyl phenyl
Benzene, [(2-chloroethyl)sulfonyl]-
NSC-145234
NSC-207409
NSC-236821
2-Chloroethyl phenyl sulphone
2-Chloroethylphenylsulfone
2-chloroethylphenyl sulfone
MFCD00025047
Phenyl 2-chloroethyl sulfone
(2-chloroethyl)-phenylsulfone
SCHEMBL798585
beta-Chloroethyl phenyl sulfone
Phenyl beta-chloroethyl sulfone
CHEMBL288134
(beta-chloroethylsulfonyl)benzene
1-chloro-2-phenylsulphonylethane
2-(Phenylsulfonyl)ethyl chloride
NUJGORANFDSMOL-UHFFFAOYSA-
EVR4295G77
1-Chloro-2-(phenylsulfonyl)ethane
CS-M0047
STR07209
[(2-Chloroethyl)sulfonyl]benzene #
Benzene,[(2-chloroethyl)sulfonyl]-
NSC145234
NSC207409
NSC236821
STK760846
AKOS005199255
DB-057434
NS00039649
EN300-22271
Z147642528
InChI=1/C8H9ClO2S/c9-6-7-12(10,11)8-4-2-1-3-5-8/h1-5H,6-7H2