Atomfair 2-hydroxyphenyltrifluoroborate potassium salt C6H5BF3KO

Description 2-Hydroxyphenyltrifluoroborate Potassium Salt (CAS No. 850313-92-7) is a high-purity organoboron compound with the molecular formula C6H5BF3KO . This potassium trifluoroborate salt is widely utilized in Suzuki-Miyaura cross-coupling reactions, offering excellent stability and reactivity for aryl-aryl bond formation. The presence of the hydroxyl group enhances its versatility in synthetic organic chemistry, making it a valuable intermediate for pharmaceutical and materials science research. Supplied as a crystalline solid, this reagent is rigorously tested for quality, ensuring consistent performance in demanding applications. Store under inert conditions to maintain stability.

Description

2-Hydroxyphenyltrifluoroborate Potassium Salt (CAS No. 850313-92-7) is a high-purity organoboron compound with the molecular formula C₆H₅BF₃KO. This potassium trifluoroborate salt is widely utilized in Suzuki-Miyaura cross-coupling reactions, offering excellent stability and reactivity for aryl-aryl bond formation. The presence of the hydroxyl group enhances its versatility in synthetic organic chemistry, making it a valuable intermediate for pharmaceutical and materials science research. Supplied as a crystalline solid, this reagent is rigorously tested for quality, ensuring consistent performance in demanding applications. Store under inert conditions to maintain stability.

CAS No: 850313-92-7
Molecular Formula: C6H5BF3KO
Molecular Weight: 200.01
Exact Mass: 200.0022609
Monoisotopic Mass: 200.0022609
IUPAC Name: potassium;trifluoro-(2-hydroxyphenyl)boranuide
SMILES: [B-](C1=CC=CC=C1O)(F)(F)F.[K+]
Synonyms: 2-HYDROXYPHENYLTRIFLUOROBORATE POTASSIUM SALT, 687-416-1, 850313-92-7, Potassium 2-hydroxyphenyltrifluoroborate, POTASSIUM TRIFLUORO(2-HYDROXYPHENYL)BORATE

Application

2-Hydroxyphenyltrifluoroborate potassium salt is primarily employed as a coupling partner in Suzuki-Miyaura cross-coupling reactions to synthesize biaryl compounds. Its hydroxyl group allows for further functionalization, making it useful in medicinal chemistry for drug discovery. The compound is also explored in materials science for constructing complex organic frameworks. Its stability under ambient conditions simplifies handling compared to traditional boronic acids.

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