CAS 233664-53-4 Potassium allyltrifluoroborate

NAVIGATION

Potassium allyltrifluoroborate

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Catalog Number

ACM233664534-1

CAS Number

233664-53-4

Product Name

Potassium allyltrifluoroborate

Category

Salt

Synonyms

Potassium allyltrifluoroborate, 233664-53-4, Potassium (prop-2-en-1-yl)trifluoroborate, PubChem11287, 659274_ALDRICH, AKOS013014117, AB31929, POTASSIUM TRIFLUORO(ALLYL)BORATE, RL02734, ALLYLTRIFLUOROBORATE POTASSIUM SALT, POTASSIUM 2-PROPENYLTRIFLUOROBORATE, P1480, POTASSIUM TRIFLUORO(PROP-2-ENYL)BORATE, potassium ion trifluoro(prop-2-en-1-yl)boranuide, POTASSIUM TRIFLUORO(PROP-2-EN-1-YL)BORANUIDE

IUPAC Name

potassium;trifluoro(prop-2-enyl)boranuide

Molecular Weight

147.97

Molecular Formula

C₃H₅BF₃.K

Canonical SMILES

[B-](CC=C)(F)(F)F.[K+]

InChI Key

TVPZAMJXLCDMIT-UHFFFAOYSA-N

Melting Point

>300ºC

Purity

>95.0%(W)

Application

Potassium allyltrifluoroborate serves as a versatile and stable reagent widely utilized in various chemical reactions. It is prominently employed in catalytic allylboration and stereoselective nucleophilic addition, showcasing its efficiency in forming complex organic compounds. This compound is also integral to Pd-catalyzed heterocyclizations and oxidation reactions, including oxidative Mannich reactions, thereby contributing significantly to synthetic organic chemistry. Further extending its utility, potassium allyltrifluoroborate facilitates cross-coupling reactions, acting as a robust surrogate for boronic acids. Additionally, it is instrumental in the high-yield synthesis of homoallylic alcohols from aldehydes through Lewis acid catalysis, underscoring its role as an invaluable tool in advanced synthesis processes.

Exact Mass

148.00700

Hazard Statements

Xi: Irritant;

Safety Description

26-36/39

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