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CS-W001157 4
Total: USD 88.00

Potassium trifluoro(4-formylphenyl)borate

  • CAS No. 374564-36-0

  • Cat. No. CS-W010485
  • Purity≥98%
  • MDL No.MFCD02093980

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

Potassium trifluoro(4-formylphenyl)borate|CS-W010485

Structure of 374564-36-0

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General Information

  • CAS No. 374564-36-0
  • Cat. No. CS-W010485
  • Purity ≥98%
  • MDL No. MFCD02093980
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₅BF₃KO
  • Molecular Weight 212.02
  • Synonym(s) potassium trifluoro(4-formylphenyl)borate(1-)
  • SMILES O=CC1=CC=C([B-](F)(F)F)C=C1.[K+]

Description

Potassium trifluoro(4-formylphenyl)borate delivers a reactive boronate handle paired with an electron-deficient aryl group, enabling efficient Suzuki-Miyaura coupling under mild conditions. This bench-stable reagent integrates seamlessly into synthetic workflows requiring precise C–C bond formation.

Application

Potassium trifluoro(4-formylphenyl)borate serves as a stable, bench-ready boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. Its formyl group provides orthogonal functionality for downstream derivatization, while the trifluoroborate moiety ensures high chemoselectivity and compatibility with diverse functional groups. This reagent facilitates reliable C–C bond formation under mild conditions, making it ideal for constructing complex aryl scaffolds in medicinal chemistry and materials synthesis.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P280-P302+P352

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Computational Chemistry Data

  • TPSA   17.07
  • LogP   -1.4425
  • H_Acceptors   1
  • H_Donors   0
  • Rotatable_Bonds   2

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