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Azoles

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1

eMolecules​ Ambeed / DIchloro[bis(diphenylphosphinophenyl)ether]palladium(II) / 1g / 552681915 / A261801 / / 205319-06-8 / [null] / 715.890 / C36H28Cl2OP2Pd

Ambeed / DIchloro[bis(diphenylphosphinophenyl)ether]palladium(II) / 1g / 552681915 / A261801 / / 205319-06-8 / [null] / 715.890 / C36H28Cl2OP2Pd

ENCOMPASS_PREFERRED
2

eMolecules​ Ambeed DIchloro[bis(diphenylphosphinophenyl)ether]palladium(II) 250mg 552681913 A261801 0 000 205319-06-8 715 890 C36H28Cl2OP2Pd

Ambeed DIchloro[bis(diphenylphosphinophenyl)ether]palladium(II) 250mg 552681913 A261801 0 000 205319-06-8 715 890 C36H28Cl2OP2Pd

ENCOMPASS_PREFERRED
3

Medchemexpress LLC Potassium (bromomethyl)trifluoroborate | 888711-44-2 | MFCD09265154 | 200.84 g/mol | BrCH2BF3K | 500 G
SDP

Potassium (bromomethyl)trifluoroborate (CAS 888711-44-2) is an organoboron reagent used as a boron-containing building block in organic synthesis. It is provided as a stable potassium trifluoroborate salt that simplifies handling and storage compared with some boronic acids, and is commonly employed in palladium-catalyzed transformations and modular assembly of complex molecules.

  • Organoboron building block for cross-coupling reactions.
  • Potassium trifluoroborate salt provides enhanced stability and ease of handling.
  • Solid form suitable for accurate weighing and storage.
  • Compatible with typical palladium-catalyzed conditions used in synthesis.
  • Supplied with a specified purity; verify certificate of analysis before use.

ENCOMPASS_PREFERRED
4

Medchemexpress LLC Potassium (bromomethyl)trifluoroborate | 888711-44-2 | MFCD09265154 | 97.0% | 200.84 g·mol⁻¹ | BrCH2BF3K | 25 G
SDP

Potassium (bromomethyl)trifluoroborate is an organotrifluoroborate salt used as an organoboron reagent in organic synthesis and medicinal chemistry research. It functions as a stable, isolable boron-containing building block for cross-coupling and functionalization reactions and is supplied for research use only.

  • Stable organotrifluoroborate salt suitable for handling and storage.
  • Provides a bromomethyl boron synthon for cross-coupling reactions.
  • Compatible with common palladium-catalyzed coupling protocols.
  • Useful as a building block in medicinal and synthetic chemistry research.
  • Supplied in small laboratory quantities for research applications.

ENCOMPASS_PREFERRED