Description
Potassium (4-Fluorophenyl)trifluoroborate (CAS No. 192863-35-7) is a high-purity organoboron compound with the molecular formula C6H4BF4K. This white to off-white crystalline powder is widely utilized in Suzuki-Miyaura cross-coupling reactions as a stable and efficient boronic acid surrogate. With a molecular weight of 194.00 g/mol, it offers excellent solubility in polar organic solvents such as DMF, DMSO, and methanol while remaining stable to air and moisture. Our product is rigorously tested to meet >98% purity standards (HPLC) and is packaged under inert atmosphere to ensure long-term stability. Ideal for pharmaceutical intermediates, material science research, and catalyst development, this reagent is supplied with comprehensive analytical data including 1H NMR, 13C NMR, and FT-IR spectra. Available in research (5g, 25g) and bulk quantities (100g, 500g, 1kg), each batch is accompanied by a Certificate of Analysis detailing purity, heavy metal content, and residual solvent levels.
Properties
- CAS Number: 192863-35-7
- Complexity: 130
- IUPAC Name: potassium;trifluoro-(4-fluorophenyl)boranuide
- InChI: InChI=1S/C6H4BF4.K/c8-6-3-1-5(2-4-6)7(9,10)11;/h1-4H;/q-1;+1
- InChI Key: PXKNUQDMYBUYSZ-UHFFFAOYSA-N
- Exact Mass: 201.9979244
- Molecular Formula: C6H4BF4K
- Molecular Weight: 202.00
- SMILES: [B-](C1=CC=C(C=C1)F)(F)(F)F.[K+]
- Monoisotopic Mass: 201.9979244
- Synonyms: Potassium (4-fluorophenyl)trifluoroborate, 681-607-3, 192863-35-7, Potassium 4-fluorophenyltrifluoroborate, Potassium trifluoro(4-fluorophenyl)borate, MFCD01318170, Borate(1-), trifluoro(4-fluorophenyl)-, potassium (1:1), (T-4)-, potassium;trifluoro-(4-fluorophenyl)boranuide, POTASSIUM TRIFLUORO(4-FLUOROPHENYL)BORANUIDE, Potassium-4-fluorophenyltrifluoroborate, 4-FLUOROPHENYLTRIFLUOROBORIC ACID POTASSIUM SALT, SCHEMBL1560330, DTXSID30635526, SBB092841, AKOS005254995, AB08666, AS-2582, Potassiumtrifluoro(4-fluorophenyl)borate, SY062257, DB-044814, CS-0137898, P1465, potassium,trifluoro-(4-fluorophenyl)boranuide, Potassium trifluoro(4-fluorophenyl)borate(1-), N11985, EN300-1253181
This reagent serves as a key building block in pharmaceutical synthesis, particularly for creating fluorinated biphenyl derivatives via palladium-catalyzed cross-coupling reactions. Its enhanced stability compared to boronic acids makes it valuable for multi-step synthetic sequences. Researchers employ it in material science for developing fluorinated organic semiconductors and liquid crystal compounds. The compound also finds use in PET radiotracer development due to the 19F moiety’s NMR activity.
Safety and Hazards
GHS Hazard Statements
- H315 (97.8%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (97.8%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
- H335 (95.6%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Precautionary Statements
- P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
Hazard Classes and Categories
- Skin Irrit. 2 (97.8%)
- Eye Irrit. 2 (97.8%)
- STOT SE 3 (95.6%)
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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