Sulprostone

Borane dimethyl sulfide complex (BMS) is a commonly used reagent and a mediator for hydroboration reaction for the preparation of organoborane compounds, which are utilized as key intermediates in organic synthesis. BMS is also employed as a

Borane dimethyl sulfide complex (BMS) is a commonly used reagent and a mediator for hydroboration reaction for the preparation of organoborane compounds, which are utilized as key intermediates in organic synthesis. BMS is also employed as a

Borane dimethyl sulfide complex (BMS) acts as a highly efficient and selective reducing agent in the presence of catalytic sodium tetrahydroborate for &#945-hydroxy esters. Asymmetric borane reduction of a variety of prochiral ketones with BMS

Borane dimethyl sulfide complex (BMS) acts as a highly efficient and selective reducing agent in the presence of catalytic sodium tetrahydroborate for &#945-hydroxy esters. Asymmetric borane reduction of a variety of prochiral ketones with BMS

Borane dimethyl sulfide complex (BMS) acts as a highly efficient and selective reducing agent in the presence of catalytic sodium tetrahydroborate for &#945-hydroxy esters. Asymmetric borane reduction of a variety of prochiral ketones with BMS

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product, 1.

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product, 1.

Application for complexometry

Application for complexometry

Cyclohexene sulfide

Application Reactant for: Reductive elimination C-C bond forming reactions Lithiation-borylation reaction with Hoppe&#8242s lithiated carbamates Preparation of boron analogues of uracil Boronation reactions for formation of cyclic boronium salts

Application Reactant for: Reductive elimination C-C bond forming reactions Lithiation-borylation reaction with Hoppe&#8242s lithiated carbamates Preparation of boron analogues of uracil Boronation reactions for formation of cyclic boronium salts