105560-52-9 | Potassium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate

Packsize	Purity	Availability	Price	Discounted Price
50mg	97%	in stock	$78.00	$55.00
100mg	97%	in stock	$129.00	$91.00
250mg	97%	in stock	$222.00	$156.00
1g	97%	in stock	$597.00	$418.00

Description

• Catalog Number: AE18411
• Chemical Name: Potassium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate
• CAS Number: 105560-52-9
• Molecular Formula: C32H12BF24K
• Molecular Weight: 902.3087
• MDL Number: MFCD00077934
• SMILES: FC(c1cc(cc(c1)C(F)(F)F)[B-](c1cc(cc(c1)C(F)(F)F)C(F)(F)F)(c1cc(cc(c1)C(F)(F)F)C(F)(F)F)c1cc(cc(c1)C(F)(F)F)C(F)(F)F)(F)F.[K+]

Upstream Synthesis Route

Potassium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate, also known as $name$, is a highly versatile compound widely utilized in chemical synthesis processes. Its unique properties make it an indispensable reagent in various reactions, particularly in organometallic chemistry and catalysis.One of the key applications of $name$ in chemical synthesis is its role as a powerful nucleophilic agent. Due to the presence of the boron atom, $name$ exhibits strong nucleophilic behavior, allowing it to participate in a wide range of reactions, such as Suzuki and Heck couplings. These reactions are fundamental in modern organic synthesis, enabling the construction of complex molecular structures efficiently.Moreover, $name$ is valued for its ability to stabilize reactive intermediates in organic reactions. By forming stable complexes with key reaction intermediates, $name$ facilitates challenging transformations that would otherwise be difficult to achieve. This feature enhances the efficiency and selectivity of various chemical reactions, making $name$ a valuable tool for synthetic chemists.Additionally, $name$ can act as a Lewis acid catalyst in certain reactions, promoting bond formations and facilitating rearrangements. Its unique electronic properties, stemming from the trifluoromethylphenyl ligands, enable precise control over reaction pathways and product distributions. This catalytic activity broadens the scope of chemical transformations that can be accomplished using $name$, further highlighting its significance in chemical synthesis.In summary, $name$ plays a crucial role in chemical synthesis by serving as a versatile nucleophilic agent, stabilizing reactive intermediates, and acting as a Lewis acid catalyst. Its diverse applications make it an essential component in the toolkit of synthetic chemists striving to develop novel molecules and materials.