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CS-W001157 4
Total: USD 88.00

3-Ethoxycarbonylphenylboronic acid

  • CAS No. 4334-87-6

  • Cat. No. CS-W015758
  • Purity≥98%
  • MDL No.MFCD02179444

*For research and further manufacturing use only, not for direct human use.

3-Ethoxycarbonylphenylboronic acid|CS-W015758

Structure of 4334-87-6

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General Information

  • CAS No. 4334-87-6
  • Cat. No. CS-W015758
  • Purity ≥98%
  • MDL No. MFCD02179444
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₁BO₄
  • Molecular Weight 193.99
  • Synonym(s) None
  • SMILES CCOC(C1=CC(=CC=C1)B(O)O)=O

Description

Reactant for:Palladium-catalyzed Suzuki-Miyaura couplingPalladium-catalyzed arylation of aldehydesReductive cross coupling reactionsPreparation of 3-adrenergic receptor agonistTransmetalation reactions

Application

3-Ethoxycarbonylphenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its ethoxycarbonyl group provides a handle for further derivatization, while the boronic acid functionality offers excellent stability, ease of purification, and compatibility with diverse functional groups. This reagent is particularly valuable for constructing substituted aromatic scaffolds in pharmaceutical and agrochemical research.

Synthesis

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      64-17-5
    • In-stock
      3-Carboxyphenylboronic acid|CS-W019968
      25487-66-5
    • ~%
    • In-stock
      3-Ethoxycarbonylphenylboronic acid|CS-W015758
      4334-87-6

    References

    • Kuivila; Hendrickson Journal of the American Chemical Society, 1952 , vol. 74, p. 5068 Full Text View citing articles Show Details Torssell et al. Arkiv foer Kemi, 1957 , vol. 10, p. 497,503

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501

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Computational Chemistry Data

  • TPSA   66.76
  • LogP   -0.4569
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   3

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