CAS 269410-16-4
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4 produits concernés.
4-Methoxynaphthalen-1-ylboronic acid pinacol ester
CAS :Formule :C17H21BO3Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :284.15782-(4-Methoxynaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS :2-(4-Methoxynaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneFormule :C17H21BO3Degré de pureté :98%Couleur et forme : beige solidMasse moléculaire :284.16g/mol2-(4-Methoxynaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS :Degré de pureté :98%Masse moléculaire :284.16000372-(4-Methoxynaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS :<p>2-(4-Methoxynaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a photochromic dioxaborolane. When irradiated with ultraviolet light of a wavelength of 365 nm, it undergoes an intramolecular cyclization to form a naphthopyran. It can be used as a pinacol ester in the synthesis of branched chain methylmagnesium compounds and halogenated naphthols. This compound is not reactive with acid dimethyl esters such as ethyl acetate. 2-(4-Methoxynaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is prepared by reacting 4-(methoxy)naphthalene with boron trifluoride etherate in</p>Formule :C17H21BO3Degré de pureté :Min. 95%Masse moléculaire :230.11 g/mol
