C11H15BBrNO2
283.96 g/mol
Research ReagentDanger
2-Bromo-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
CAS651358-83-7EC676-788-0
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound
This compound is a boronic ester derivative used as a cross-coupling reagent in organic synthesis. It features a brominated pyridine ring and is commonly employed in laboratory research for constructing carbon-carbon bonds.
cross-coupling reagent in organic synthesislaboratory research reagent
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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CAS 651358-83-7
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Referencesame scaffold
Pyridine-2-boronic acid pinacol ester
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Safety Reference
Danger
H301Toxic if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
Identifiers
IUPAC Name
2-bromo-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
InChIKey
OAVRLCKBKDMGGW-UHFFFAOYSA-N
SMILES
B1(OC(C(O1)(C)C)(C)C)C2=NC(=CC=C2)Br
Synonyms (8)
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