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CS-W001157 4
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Potassium cyclohexylmethyltrifluoroborate

  • CAS No. 1346647-18-4

  • Cat. No. CS-0207562
  • Purity≥98%
  • MDL No.MFCD11052658

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

Potassium cyclohexylmethyltrifluoroborate|CS-0207562

Structure of 1346647-18-4

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General Information

  • CAS No. 1346647-18-4
  • Cat. No. CS-0207562
  • Purity ≥98%
  • MDL No. MFCD11052658
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₁₃BF₃K
  • Molecular Weight 204.08
  • Synonym(s) Potassium cyclohexylmethyltrilfuoroborate
  • SMILES C1CCC(CC1)C[B-](F)(F)F.[K+]

Description

Potassium cyclohexylmethyltrifluoroborate delivers a stable, bench-ready trifluoroborate handle for cross-coupling reactions. This reagent features a sterically protected cyclohexylmethyl moiety that enhances functional group tolerance and reduces protodeboronation. It integrates seamlessly into Suzuki-Miyaura protocols under standard conditions, enabling efficient C–C bond formation with aryl and heteroaryl halides.

Application

Potassium cyclohexylmethyltrifluoroborate serves as a stable, bench-ready boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. Its trifluoroborate group offers enhanced hydrolytic stability and functional group tolerance compared to traditional boronic acids, facilitating reliable C–C bond formation under mild conditions. This reagent functions effectively in diverse coupling protocols with aryl, heteroaryl, and vinyl halides, supporting scalable synthesis of complex molecular architectures.

Safety Information

Download SDS
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   0
  • LogP   0.4181
  • H_Acceptors   0
  • H_Donors   0
  • Rotatable_Bonds   2

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