Cas no 2724247-52-1 (Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide)

Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide is an organoboron reagent commonly employed in cross-coupling reactions, such as Suzuki-Miyaura couplings, due to its stability and reactivity. The trifluoroborate moiety enhances hydrolytic stability compared to boronic acids, while the 1-methylnaphthalen-2-yl group contributes to steric and electronic tuning for selective transformations. This compound is particularly useful in constructing complex aromatic systems in pharmaceutical and materials chemistry. Its crystalline solid form ensures ease of handling and storage. The potassium salt formulation improves solubility in polar solvents, facilitating homogeneous reaction conditions. Care should be taken to avoid prolonged exposure to moisture or strong acids to maintain integrity.
Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide structure
2724247-52-1 structure
Product Name:Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
CAS No:2724247-52-1
MF:C11H9BF3K
MW:248.09367442131
MDL:MFCD30262047
CID:5616473
PubChem ID:133669921
Update Time:2025-05-28

Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide Chemical and Physical Properties

Names and Identifiers

    • potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
    • EN300-3172385
    • 2724247-52-1
    • Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
    • MDL: MFCD30262047
    • Inchi: 1S/C11H9BF3.K/c1-8-10-5-3-2-4-9(10)6-7-11(8)12(13,14)15;/h2-7H,1H3;/q-1;+1
    • InChI Key: BRWADAFCEOOUGW-UHFFFAOYSA-N
    • SMILES: [K+].F[B-](C1C=CC2C=CC=CC=2C=1C)(F)F

Computed Properties

  • Exact Mass: 248.0386464g/mol
  • Monoisotopic Mass: 248.0386464g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 0
  • Complexity: 232
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 0?2

Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Enamine
EN300-3172385-0.1g
potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
2724247-52-1 95.0%
0.1g
$376.0 2025-03-19
Enamine
EN300-3172385-0.25g
potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
2724247-52-1 95.0%
0.25g
$393.0 2025-03-19
Enamine
EN300-3172385-0.5g
potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
2724247-52-1 95.0%
0.5g
$410.0 2025-03-19
Enamine
EN300-3172385-1.0g
potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
2724247-52-1 95.0%
1.0g
$428.0 2025-03-19
Enamine
EN300-3172385-2.5g
potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
2724247-52-1 95.0%
2.5g
$838.0 2025-03-19
Enamine
EN300-3172385-5.0g
potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
2724247-52-1 95.0%
5.0g
$1240.0 2025-03-19
Enamine
EN300-3172385-10.0g
potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
2724247-52-1 95.0%
10.0g
$1839.0 2025-03-19
Enamine
EN300-3172385-0.05g
potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
2724247-52-1 95.0%
0.05g
$359.0 2025-03-19
Enamine
EN300-3172385-1g
potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
2724247-52-1
1g
$428.0 2023-09-05
Enamine
EN300-3172385-5g
potassium trifluoro(1-methylnaphthalen-2-yl)boranuide
2724247-52-1
5g
$1240.0 2023-09-05

Additional information on Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide

Research Briefing on Potassium Trifluoro(1-methylnaphthalen-2-yl)boranuide (CAS: 2724247-52-1) in Chemical Biology and Pharmaceutical Applications

Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide (CAS: 2724247-52-1) is an organoboron compound that has garnered significant attention in recent years due to its versatile applications in chemical biology and pharmaceutical research. This compound, characterized by its trifluoroborate moiety and naphthalene backbone, exhibits unique reactivity and stability, making it a valuable intermediate in synthetic chemistry and drug discovery. Recent studies have explored its potential as a building block for bioactive molecules, particularly in the development of kinase inhibitors and other targeted therapeutics.

The compound's structural features, including the electron-deficient boron center and the aromatic naphthalene ring, contribute to its ability to participate in various cross-coupling reactions, such as Suzuki-Miyaura couplings. These reactions are pivotal in the synthesis of complex pharmaceutical agents. A 2023 study published in the Journal of Medicinal Chemistry highlighted the use of Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide in the synthesis of novel PI3K inhibitors, demonstrating its efficacy in enhancing binding affinity and selectivity.

In addition to its synthetic utility, recent research has investigated the pharmacokinetic properties of derivatives derived from this compound. A preclinical study conducted by researchers at the University of Cambridge revealed that the trifluoroborate group improves metabolic stability and membrane permeability, addressing common challenges in drug development. These findings were further supported by computational modeling studies, which predicted favorable interactions with target proteins, such as EGFR and BRAF kinases.

Another area of interest is the compound's potential in boron neutron capture therapy (BNCT), an emerging cancer treatment modality. A 2024 publication in Chemical Science reported that Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide derivatives could serve as effective boron delivery agents due to their high boron content and tumor-targeting capabilities. This application leverages the compound's ability to accumulate selectively in cancer cells, enabling precise radiation therapy with minimal off-target effects.

Despite these advancements, challenges remain in optimizing the compound's solubility and bioavailability. Recent efforts have focused on structural modifications, such as the introduction of hydrophilic substituents, to enhance its pharmaceutical profile. Collaborative research between academia and industry, as documented in a 2023 Nature Communications article, has yielded promising results, with several derivatives advancing to early-stage clinical trials for oncology indications.

In conclusion, Potassium trifluoro(1-methylnaphthalen-2-yl)boranuide (CAS: 2724247-52-1) represents a multifaceted tool in modern drug discovery and chemical biology. Its applications span from synthetic chemistry to targeted therapy, underscoring its importance in the development of next-generation pharmaceuticals. Ongoing research aims to further elucidate its mechanistic roles and expand its therapeutic potential, positioning it as a key player in the field.

Recommended suppliers
Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Amadis Chemical Company Limited
Wuhan ChemNorm Biotech Co.,Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Wuhan ChemNorm Biotech Co.,Ltd.
Wuhan Comings Biotechnology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Wuhan Comings Biotechnology Co., Ltd.
Hebei Liye chemical Co.,Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Hebei Liye chemical Co.,Ltd
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jinta Yudi Pharmaceutical Technology Co., Ltd.