Potassium Vinyltrifluoroborate丨CAS 13682-77-4

Potassium Vinyltrifluoroborate丨CAS 13682-77-4
Product Introduction:
Catalog No.: SS131702
CAS No.: 13682-77-4
Purity: 97% min; QNMR: 95% min
Product Name: Potassium vinyltrifluoroborate
Molecular Formula: C2H3BF3K
Molecular Weight: 133.95
Synonym(s): Potassium trifluoro(vinyl)borate; Potassium (ethenyl)trifluoroborate
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Technical Parameters
Description

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Specifications

 

Appearance White to off-white powder
Purity 97% min
QNMR 95% min
1H NMR δ ppm 5.82-5.70 (m, 1 H), 5.11-5.05 (m, 2 H)
Solubility - DMSO 25 mg/ml min
Solubility - MeOH 25 mg/ml min
Residue on ignition 0.5% max
Water 1.0% max

 

Transport Information

 

Parameter

Specification

UN Number

 

Class

 

Packing Group

 

H.S. Code

2931900090999

Stability & Reactivity

The product is chemically stable under standard ambient conditions.

Storage

Keep container tightly closed. Store in a cool and shaded area. Protect from moisture. Keep under inert gas

Condition to Avoid

Exposure to air. Exposure to moisture

Package

 

 

Manufacturing Information

 

Parameter

Specification

Capacity

10MT/year

Frequency

 

Main Export Countries

 

Capacity/Batch

 

Experience

Production since 2014

Stock

 

 

 

 

Applications

 

Potassium vinyltrifluoroborate (CAS 13682-77-4) is an organoboron compound widely used as a reagent and intermediate in organic synthesis, particularly in cross-coupling reactions. Its primary applications include serving as a vinyl source in Suzuki–Miyaura coupling reactions to construct carbon–carbon double bonds, enabling the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and fine chemicals. It is also utilized in the preparation of functionalized alkenes, heterocycles, and polymer precursors. Its stability, ease of handling, and water solubility make it an attractive alternative to traditional vinylboronic acids or esters in synthetic chemistry.

 

Benefits

 

The benefits of potassium vinyltrifluoroborate stem from its chemical stability, reactivity, and versatility. Unlike many boronic acids, it is air- and moisture-stable, allowing safe storage and handling in the laboratory. Its reactivity in palladium-catalyzed cross-coupling reactions provides high yields and selectivity under mild conditions. Additionally, the trifluoroborate group improves solubility and reduces protodeboronation side reactions, ensuring reproducible and efficient transformations. These properties make it a valuable tool for synthesizing complex molecules with precise control over structure and functionality.

 

Conclusion

 

In conclusion, potassium vinyltrifluoroborate is a reliable and versatile organoboron reagent for modern organic synthesis. Its stability, reactivity, and compatibility with cross-coupling methods make it ideal for producing pharmaceuticals, fine chemicals, and advanced materials. By enabling efficient and selective carbon–carbon bond formation, it plays a key role in contemporary synthetic and medicinal chemistry.

 

 

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