Cas no 1451393-06-8 ((4-Bromo-2-fluoro-3-formylphenyl)boronic acid)

(4-Bromo-2-fluoro-3-formylphenyl)boronic acid is a versatile boronic acid derivative widely used in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Its bromo and fluoro substituents enhance reactivity and selectivity, while the formyl group offers additional functionalization potential. This compound is particularly valuable in pharmaceutical and materials science research, where precise structural modifications are required. Its stability under typical reaction conditions and compatibility with various catalysts make it a reliable intermediate for constructing complex aromatic frameworks. High purity grades ensure consistent performance in demanding applications. Proper handling under inert conditions is recommended to maintain its integrity.
(4-Bromo-2-fluoro-3-formylphenyl)boronic acid structure
1451393-06-8 structure
Product Name:(4-Bromo-2-fluoro-3-formylphenyl)boronic acid
CAS No:1451393-06-8
MF:C7H5BBrFO3
MW:246.826205015182
MDL:MFCD16295245
CID:4733025
Update Time:2025-10-29

(4-Bromo-2-fluoro-3-formylphenyl)boronic acid Chemical and Physical Properties

Names and Identifiers

    • 4-Bromo-2-fluoro-3-formylphenylboronic acid
    • (4-Bromo-2-fluoro-3-formylphenyl)boronic acid
    • BC001705
    • Z1481
    • MDL: MFCD16295245
    • Inchi: 1S/C7H5BBrFO3/c9-6-2-1-5(8(12)13)7(10)4(6)3-11/h1-3,12-13H
    • InChI Key: UIXKWZUGARWZOM-UHFFFAOYSA-N
    • SMILES: BrC1C=CC(B(O)O)=C(C=1C=O)F

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 2
  • Complexity: 193
  • Topological Polar Surface Area: 57.5

(4-Bromo-2-fluoro-3-formylphenyl)boronic acid Pricemore >>

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