2-Methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boronic ester compound commonly used as a research reagent in organic synthesis. Its primary significance lies in its role as a building block for cross-coupling reactions and other synthetic transformations.
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CAS 1195-66-0
N6-(N-Threonylcarbonyl)adenosine-13C4,15N
Stable isotope labeled reference standard
Acyclovir Impurity 32
pharmaceutical impurity reference standard
N-{3-[5-(2-chloro-4-pyrimidinyl)-2-(1,1-diethylethyl)-1,3-thiazol-4-yl]-2-fluoraphenyl}-2,6-difluorobenzenesulfonamide
research compound
(1S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carbonyl chloride
research compound
4,4,5,5-Tetramethyl-2-(2-methylprop-1-en-1-yl)-1,3,2-dioxaborolane
Boronic ester for Suzuki coupling
4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane
boronic ester research reagent
3-methyl-1-(tetramethyl-1,3,2-dioxaborolan-2-yl)butan-1-amine hydrochloride
pharmaceutical intermediate
(E)-ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)acrylate
n.a
2-methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
JZZJAWSMSXCSIB-UHFFFAOYSA-N
B1(OC(C(O1)(C)C)(C)C)OC
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