Alkylating agent alkanesulfonic acids

Application Reactant involved in: Oxidative hydroxylation for the preparation of phenols Homolytic aromatic substitution Cross-coupling with &#945-bromocarbonyl compounds Suzuki-coupling reaction with quinoline carboxylates Trifluoromethylation

Application 4-Ethylbenzenesulfonic acid was used to dope high conducting polypyrrole thin films .

4-Fluorobenzenesulfonyl isocyanate

4-Fluorobenzenesulfonyl isocyanate

Application 4-Formylphenylboronic acid is a substrate for Suzuki cross-coupling reactions and it can be used as a reagent for: Palladium-catalyzed Suzuki-Miyaura cross-coupling in water. Copper-mediated ligandless aerobic fluoroalkylation of

Application 4-Formylphenylboronic acid is a substrate for Suzuki cross-coupling reactions and it can be used as a reagent for: Palladium-catalyzed Suzuki-Miyaura cross-coupling in water. Copper-mediated ligandless aerobic fluoroalkylation of

Application 4-Formylphenylboronic acid is a substrate for Suzuki cross-coupling reactions and it can be used as a reagent for: Palladium-catalyzed Suzuki-Miyaura cross-coupling in water. Copper-mediated ligandless aerobic fluoroalkylation of

4-Hydroxybenzenesulfonic acid solution

4-Hydroxybenzenesulfonic acid solution

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