Alkylating agent alkanesulfonic acids

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application Reactant for preparation of biologically active molecules: Preparation of hydroxyphenylnaphthols as 17ß-hydroxysteroid dehydrogenase Type 2 inhibitors Reactant for: Preparation of axially-chiral biarylphosphonates by asymmetric Suzuki

Application Reagent used for Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides One-pot ipso-nitration of

Application Reagent used for Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides One-pot ipso-nitration of

4-methylbenzenesulfinic acid.

4-methylbenzenesulfinic acid.

4-Methylbenzenesulfinic acid.

4-Methylbenzenesulfinic acid.

4-Methylbenzenesulfinic acid.

4-Toluenesulfonic acid.

Application 4-Vinylphenylboronic acid is commonly used in the synthesis of styrene-based organoboron polymers such as vinyl-oligo(fluorene) polymer and boronic ester based self-healing polymer. It can also be used as a precursor in the synthesis of

Application 4-Vinylphenylboronic acid is commonly used in the synthesis of styrene-based organoboron polymers such as vinyl-oligo(fluorene) polymer and boronic ester based self-healing polymer. It can also be used as a precursor in the synthesis of