2-Chloroethyl benzenesulfonate, with the CAS number 16670-48-7, is an organic compound characterized by the presence of a chloroethyl group and a benzenesulfonate moiety. It typically appears as a colorless to pale yellow liquid and is known for its reactivity, particularly as an alkylating agent. The compound features a sulfonate group, which enhances its solubility in polar solvents, making it useful in various chemical reactions. It is often employed in organic synthesis, particularly in the preparation of sulfonamide derivatives and other functionalized compounds. Due to the presence of the chloroethyl group, it can participate in nucleophilic substitution reactions, making it valuable in medicinal chemistry and the development of pharmaceuticals. However, it is important to handle this compound with care, as it may pose health risks, including potential toxicity and environmental hazards. Proper safety measures should be observed when working with 2-chloroethyl benzenesulfonate in laboratory settings.

2-Chloroethyl benzenesulfonate

16670-48-7: 2-(Benzene-sulphonyloxy)ethyl chloride, 2-Chloroethanol benzenesulfonate, 2-Chloroethyl Benzenesulfonate, 2-Chloroethyl Benzenesulfonate,98.0%(Gc), Ethanol, 2-chloro-, 1-benzenesulfonate, Ethanol, 2-chloro-, benzenesulfonate, β-Chloroethyl benzenesulfonate

2-Chloroethyl Benzenesulfonate

Ethanol, 2-chloro-, 1-benzenesulfonate

2-Chloroethyl benzenesulfonate is a synthetic compound that has been used as an intermediate for the synthesis of tamoxifen and analogues. It can be used in the synthesis of amines, phenolic compounds, and pyrylium salts. 2-Chloroethyl benzenesulfonate has anticancer effects and can also be used to synthesize drugs with anticancer activity.

CAS 16670-48-7: 2-Chloroethyl benzenesulfonate

2-Chloroethyl Benzenesulfonate

Ref: 3B-C2230

Ethanol, 2-chloro-, 1-benzenesulfonate

Ref: IN-DA001WWG

2-Chloroethyl benzenesulfonate

Ref: 10-F770782

2-Chloroethyl Benzenesulfonate

Ref: 3D-RAA67048