Alkylating agent alkanesulfonic acids

The fluorescence of 2-naphthalenesulfonic acid (NSA) is effectively quenched by colloidal silver via photoinduced interfacial electron transfer from the excited singlet of NSA to silver . Adsorption behavior of NSA on a conventional macroporous

Application Used in a study of an enantioselective rhodium-catalyzed addition of aryl boronic acids to 2,2,2-trifluoroacetophenones leading to chiral, tertiary trifluoromethyl alcohols. Also employed in a study of a palladium-catalyzed addition of

Application Used in a study of an enantioselective rhodium-catalyzed addition of aryl boronic acids to 2,2,2-trifluoroacetophenones leading to chiral, tertiary trifluoromethyl alcohols. Also employed in a study of a palladium-catalyzed addition of

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.

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 3,4-Dimethoxyphenylboronic acid can be used: As a substrate in the cross-coupling reaction with 5,7-dichloropyrido[4,3- d ]pyrimidine catalyzed by palladium. As a starting material for the synthesis of buflavine 1, a natural alkaloid.

Application 3,4-Dimethoxyphenylboronic acid can be used: As a substrate in the cross-coupling reaction with 5,7-dichloropyrido[4,3- d ]pyrimidine catalyzed by palladium. As a starting material for the synthesis of buflavine 1, a natural alkaloid.

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.

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: Palladium-catalyzed Suzuki-Miyaura coupling Palladium-catalyzed arylation of aldehydes Reductive cross coupling reactions Preparation of &#9463-adrenergic receptor agonist Transmetalation reactions Other Notes Contains

Application Used as a lubricating additive in grease for reducing fretting wear Other Notes May contain varying amounts of anhydride

Application Reagent used: To study the effects of boronic acid on fluoride-selective chemosignaling behavior of merocyanine dye As exciton-coupled CD probes for epigallocatechin gallate Biological inhibitor of &#947-glutamyltranspeptidase Reactant