2-Isopropoxyethyl 4-methylbenzenesulfonate, with the CAS number 51218-98-5, is an organic compound characterized by its sulfonate functional group, which contributes to its solubility in polar solvents. This compound features an isopropoxyethyl group, indicating the presence of an isopropyl ether moiety, which enhances its reactivity and potential applications in organic synthesis. The 4-methylbenzenesulfonate part of the molecule suggests that it has aromatic characteristics, which can influence its stability and reactivity. Typically, sulfonates like this one are used as intermediates in the synthesis of various chemical products, including pharmaceuticals and agrochemicals. The compound is likely to be a colorless to pale yellow liquid, with a moderate boiling point and density, and it may exhibit moderate toxicity, necessitating careful handling. Its reactivity can be attributed to the sulfonate group, which can participate in nucleophilic substitution reactions, making it a valuable building block in synthetic organic chemistry.

2-isopropoxyethyl 4-methylbenzenesulfonate

51218-98-5: 2-Isopropoxyethyl 4-methylbenzenesulfonate, with the CAS number 51218-98-5, is an organic compound characterized by its sulfonate functional group, which contributes to its solubility in polar solvents. This compound features an isopropoxyethyl group, indicating the presence of an isopropyl ether moiety, which enhances its reactivity and potential applications in organic synthesis. The 4-methylbenzenesulfonate part of the molecule suggests that it has aromatic characteristics, which can influence its stability and reactivity. Typically, sulfonates like this one are used as intermediates in the synthesis of various chemical products, including pharmaceuticals and agrochemicals. The compound is likely to be a colorless to pale yellow liquid, with a moderate boiling point and density, and it may exhibit moderate toxicity, necessitating careful handling. Its reactivity can be attributed to the sulfonate group, which can participate in nucleophilic substitution reactions, making it a valuable building block in synthetic organic chemistry.

CAS 51218-98-5

2-isopropoxyethyl 4-methylbenzenesulfonate

Ethanol, 2-(1-methylethoxy)-, 4-methylbenzenesulfonate

Ref: IN-DA00I965