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Ethyl Benzenesulfonate

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Identification
Molecular formula
C8H10O3S
CAS number
515-80-4
IUPAC name
ethyl benzenesulfonate
State
State

Ethyl benzenesulfonate is in a liquid state at room temperature.

Melting point (Celsius)
-17.50
Melting point (Kelvin)
255.65
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
200.25g/mol
Molar mass
200.2450g/mol
Density
1.1833g/cm3
Appearence

Ethyl benzenesulfonate is typically a colorless to pale yellow liquid. It has no distinct odor and appears clear.

Comment on solubility

Solubility of Ethyl Benzenesulfonate

Ethyl benzenesulfonate, with the chemical formula C8H10O3S, exhibits intriguing solubility characteristics that are important to consider in various chemical applications.

Key Solubility Insights:

  • Polarity: Ethyl benzenesulfonate is a polar organic compound due to the presence of the sulfonate group. This polarity enhances its solubility in polar solvents.
  • Solvent Compatibility: It is generally soluble in water due to its polar nature, but the solubility may be affected by temperature and pH factors.
  • Organic Solvents: This compound is also soluble in many organic solvents, including alcohols and ethers, which allows for versatility in chemical reactions.
  • Applications: The solubility of ethyl benzenesulfonate in various media makes it useful in synthesis and industrial applications.

In conclusion, the solubility of ethyl benzenesulfonate is affected by its polar characteristics, making it an important component in both inorganic and organic chemistry. Understanding its solubility can aid in optimizing processes and reactions involving this compound.

Interesting facts

Interesting Facts about Ethyl Benzenesulfonate

Ethyl benzenesulfonate, an aromatic sulfonate ester, is fascinating in several ways due to its unique chemical structure and diverse applications in various fields.

Chemical Properties and Structure

The compound consists of a benzene ring bonded to an ethyl group and a sulfonate group (SO3), embodying a fascinating interplay between organic and inorganic chemistry. Some notable aspects include:

  • Reactivity: Ethyl benzenesulfonate can act as a versatile electrophile in nucleophilic substitution reactions.
  • Synthesis: It can be synthesized by sulfonation of ethyl benzene, showcasing methods of functional group transformation.
  • Stability: The sulfonate group enhances the compound's overall chemical stability compared to alkyl halides.

Applications

The utility of ethyl benzenesulfonate is evident in several applications:

  • Organic Synthesis: It is widely used as an intermediate in the synthesis of pharmaceuticals and agrochemicals.
  • Production of Surfactants: Ethyl benzenesulfonate plays a role in the manufacturing of:
    • Detergents
    • Emulsifiers

Biological Importance

Interestingly, compounds like ethyl benzenesulfonate can:

  • Exhibit antimicrobial properties, which makes them valuable in medicinal chemistry.
  • Interact with biological systems, allowing for studies into drug design and delivery.

In summary, ethyl benzenesulfonate stands out as a notable compound in both chemical synthesis and potential biomedical applications. Its diverse reactivity and range of uses can stimulate further research and innovation in the field of chemistry.

Synonyms
ETHYL BENZENESULFONATE
515-46-8
Ethyl benzenesulphonate
Benzenesulfonic acid ethyl ester
Benzenesulfonic acid, ethyl ester
Ethyl Phenylsulfonate
CCRIS 9155
EINECS 208-200-1
09424QHU6Q
NSC-3217
DTXSID7075428
NSC 3217
BENZENESULFONIC ACID ETHYL ESTER [MI]
DTXCID4041028
Ethyl benzensulfonate
MFCD00025033
UNII-09424QHU6Q
ethoxysulfonylbenzene
ethyl benzene sulfonate
SCHEMBL347302
XDRMBCMMABGNMM-UHFFFAOYSA-
NSC3217
AC8062
STL280533
AKOS006230587
DS-6022
SY053068
DB-051985
B0032
NS00032300
Q27236452
Ethyl benzenesulfonate, certified reference material, TraceCERT(R)
InChI=1/C8H10O3S/c1-2-11-12(9,10)8-6-4-3-5-7-8/h3-7H,2H2,1H3