For research use only. Not for therapeutic Use.
2-[4-(Bromomethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(Cat No.:R019245)is a bifunctional organic compound featuring a boronic ester (dioxaborolane) and a bromomethyl-substituted phenyl ring. The boronic ester moiety makes it highly valuable in Suzuki–Miyaura cross-coupling reactions for constructing carbon–carbon bonds, especially in pharmaceutical and materials chemistry. The bromomethyl group serves as a reactive handle for further functionalization, including nucleophilic substitution and coupling. This compound, typically a stable crystalline solid, is widely used as a versatile intermediate in the synthesis of complex organic molecules, allowing modular and efficient incorporation of aromatic structures into diverse molecular frameworks.
CAS Number | 138500-85-3 |
Synonyms | 2-[4-(Bromomethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
Molecular Formula | C13H18BBrO2 |
Purity | ≥95% |
Storage | Store at +4C |
IUPAC Name | 2-[4-(bromomethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
InChI | InChI=1S/C13H18BBrO2/c1-12(2)13(3,4)17-14(16-12)11-7-5-10(9-15)6-8-11/h5-8H,9H2,1-4H3 |
InChIKey | CBUOGMOTDGNEAW-UHFFFAOYSA-N |
SMILES | B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C=C2)CBr |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |