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Atomfair 2-(4-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane C13H18BBrO2

Description 2-(4-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS No. 138500-85-3) is a high-purity boronic ester derivative with the molecular formula C13H18BBrO2. This compound features a reactive bromomethyl group and a stable dioxaborolane moiety, making it a versatile intermediate in organic synthesis and cross-coupling reactions. Its crystalline form ensures consistent performance in Suzuki-Miyaura couplings, functional group transformations, and pharmaceutical research. Ideal for researchers seeking precision in aryl boronate synthesis, this product is rigorously tested for purity (>95% by HPLC) and stored under inert conditions to maintain stability. Available in customizable quantities with detailed analytical data (NMR, MS, FTIR) upon request.

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Description

Description

2-(4-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS No. 138500-85-3) is a high-purity boronic ester derivative with the molecular formula C13H18BBrO2. This compound features a reactive bromomethyl group and a stable dioxaborolane moiety, making it a versatile intermediate in organic synthesis and cross-coupling reactions. Its crystalline form ensures consistent performance in Suzuki-Miyaura couplings, functional group transformations, and pharmaceutical research. Ideal for researchers seeking precision in aryl boronate synthesis, this product is rigorously tested for purity (>95% by HPLC) and stored under inert conditions to maintain stability. Available in customizable quantities with detailed analytical data (NMR, MS, FTIR) upon request.

  • CAS No: 138500-85-3
  • Molecular Formula: C13H18BBrO2
  • Molecular Weight: 297.00
  • Exact Mass: 296.05832
  • Monoisotopic Mass: 296.05832
  • IUPAC Name: 2-[4-(bromomethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C=C2)CBr
  • Synonyms: 138500-85-3, 2-(4-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 2-[4-(bromomethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, DTXSID00395701, DTXCID90346560

Application

This compound is widely used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for constructing biaryl structures in drug discovery. It also serves as a precursor for functionalized boronic acids in materials science and agrochemical research. The bromomethyl group enables further derivatization for targeted molecular design.

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