Skip to main content

2-chloroethyl 4-methylbenzenesulfonate

ADVERTISEMENT
Identification
Molecular formula
C9H11ClO3S
CAS number
1007-23-2
IUPAC name
2-chloroethyl 4-methylbenzenesulfonate
State
State

2-Chloroethyl 4-methylbenzenesulfonate is typically in a liquid state at room temperature. The liquid form is useful for various synthetic applications.

Melting point (Celsius)
-5.00
Melting point (Kelvin)
268.15
Boiling point (Celsius)
297.20
Boiling point (Kelvin)
570.35
General information
Molecular weight
234.69g/mol
Molar mass
234.6940g/mol
Density
1.2944g/cm3
Appearence

2-Chloroethyl 4-methylbenzenesulfonate is a colorless to light yellow liquid. It has a distinct odor and is typically used as an intermediate in chemical synthesis.

Comment on solubility

Solubility of 2-chloroethyl 4-methylbenzenesulfonate

2-chloroethyl 4-methylbenzenesulfonate, often referred to in chemical contexts, exhibits interesting solubility characteristics that are worth exploring. This compound's solubility can be influenced by various factors, including:

  • Polarity: The presence of a sulfonate group generally increases the polarity of the molecule, which can enhance its solubility in polar solvents.
  • Solvent Interaction: In polar solvents like water, the solubility is typically better due to hydrogen bonding capabilities. However, in less polar solvents, solubility may decrease.
  • Temperature Effects: Temperature can play a significant role in solubility; often, increasing the temperature will increase the solubility of many compounds.

Overall, while 2-chloroethyl 4-methylbenzenesulfonate is likely to be soluble in polar solvents, its exact solubility will depend on the specific solvation dynamics and conditions provided in a given experimentation setting. In chemical discussions, it's often emphasized, "the solvent's identity can be as important as the solute itself" due to the complex interactions at play. Therefore, further empirical studies are often necessary to quantify exact solubility values under various conditions.

Interesting facts

Interesting Facts about 2-Chloroethyl 4-Methylbenzenesulfonate

2-Chloroethyl 4-methylbenzenesulfonate is a fascinating compound that showcases the interplay of organic chemistry and its applications in various fields. Here are some engaging insights about this compound:

  • Structure and Functionality: As an organosulfonate, this compound contains both a sulfonate group and a halogen. The presence of chlorine in the 2-chloroethyl group makes it a potential electrophilic center, making it an interesting target for nucleophilic substitution reactions.
  • Synthesis: This compound can be synthesized through various methods, often involving the reaction between 4-methylbenzenesulfonyl chloride and 2-chloroethanol. Such synthesis techniques are crucial in the production of pharmaceuticals and other industrial chemicals.
  • Applications: The compound has vital uses in medicinal chemistry, particularly as an alkylating agent. Alkylating agents are important in the creation of drugs designed to target cancer cells, demonstrating the compound's role in life-saving therapies.
  • Research Interest: Its unique reactivity profile makes 2-chloroethyl 4-methylbenzenesulfonate a subject of interest in synthetic chemistry research, where scientists explore new methods of functionalization and compound modification.
  • Toxicity Considerations: As with many organochlorine compounds, appropriate safety measures must be taken when handling this compound, as it can exhibit toxicity depending on the exposure level. Proper laboratory protocols are essential to mitigate risks.

In summary, 2-chloroethyl 4-methylbenzenesulfonate encapsulates the complex world of organic compounds, illustrating how even a single structure can lead to diverse implications in both science and application. Its dynamic nature continues to inspire chemists and researchers alike.

Synonyms
80-41-1
2-Chloroethyl p-toluenesulfonate
2-Chloroethyl 4-methylbenzenesulfonate
2-Chloroethyl tosylate
2-Chloroethyl p-tosylate
2-Tosyloxyethyl chloride
Ethanol, 2-chloro-, 4-methylbenzenesulfonate
2-Chloroethanol p-toluenesulfonate
p-Toluenesulfonic acid, 2-chloroethyl ester
2-(p-Toluenesulfonyloxy)ethyl chloride
2-Chloroethyl toluene-4-sulphonate
NSC 6079
MFCD00000970
Ethanol, 2-chloro-, p-toluenesulfonate
2-chloroethyl-p-toluenesulfonate
p-Toluenesulfonic acid-2-chloroethyl ester
Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate)
2-Chlorethylester kyseliny p-toluensulfonove
DTXSID20883256
2-Chloroethyl para-toluenesulfonate
.beta.-Chloroethyl p-toluenesulfonate
2-chloroethyl 4-methylbenzene-1-sulfonate
p-Toluenesulfonic acid, .beta.-chloroethyl ester
.beta.-Chloroethylester kyseliny p-toluensulfonove
2-CHLOROETHYLP-TOLUENESULFONATE
p-Toluenesulfonic Acid 2-Chloroethyl Ester
beta-Chloroethyl p-toluenesulfonate
EINECS 201-277-2
2-Chloroethanol 4-methylbenzenesulfonate
BRN 1968816
AI3-02279
chloroethyltosylate
chloroethyl tosylate
chloroethyl-tosylate
2-Chlorethylester kyseliny p-toluensulfonove [Czech]
p-TOLUENESULFONIC ACID, beta-CHLOROETHYL ESTER
beta-Chloroethylester kyseliny p-toluensulfonove [Czech]
2-chloroethanol tosylate
beta-CHLOROETHYL-p-TOLUENE SULFONATE
2-chloro ethanol tosylate
1-chloro-2-tosyloxyethane
beta-Chloroethylester kyseliny p-toluensulfonove
WLN: G2OSWR D1
4-11-00-00249 (Beilstein Handbook Reference)
SCHEMBL263231
2-chloroethyl-p-toluensulfonate
CHEMBL166116
2-chloroethyl p-toluensulphonate
2-chloroethyl p-toluenesulphonate
2-chloroethyl-p-toluenesulphonate
ZXNMIUJDTOMBPV-UHFFFAOYSA-
2-chloroethyl-p-toluene sulfonate
2-chloroethyl-p-toluene-sulfonate
2-chloroethyl-paratoluenesulfonate
NSC6079
2-Chloroethyl p-toluene sulfonate
DTXCID501022800
beta-chloroethyl p-toluenesulphonate
NSC-6079
1-chloro-2-p-toluenesulfonyloxyethane
AKOS005258286
(2-chloro-ethyl) toluene-4-sulphonate
2-Chloroethyl p-toluenesulfonate, 97%
2-Chloroethyl 4-methylbenzenesulfonate #
MS-20213
SY048380
DB-020931
p-toluenesulfonic acid-beta-chloroethylester
toluene-4-sulfonic acid 2-chloroethyl ester
C2380
CS-0130585
NS00041075
Toluene-4-sulfonic acid 2-chloro-ethyl ester
D71096
4-methyl-benzenesulfonic acid 2-chloro-ethyl ester
201-277-2
InChI=1/C9H11ClO3S/c1-8-2-4-9(5-3-8)14(11,12)13-7-6-10/h2-5H,6-7H2,1H3