1150114-45-6 | 5-(t-Butyldimethylsilyloxy)-2,3-difluorophenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	96%	in stock	$201.00	$141.00
1g	96%	in stock	$401.00	$281.00
5g	96%	in stock	$1,535.00	$1,074.00

Description

• Catalog Number: AA20014
• Chemical Name: 5-(t-Butyldimethylsilyloxy)-2,3-difluorophenylboronic acid
• CAS Number: 1150114-45-6
• Molecular Formula: C12H19BF2O3Si
• Molecular Weight: 288.1708
• MDL Number: MFCD11855842
• SMILES: Fc1cc(cc(c1F)B(O)O)O[Si](C(C)(C)C)(C)C

Upstream Synthesis Route

The 5-(t-Butyldimethylsilyloxy)-2,3-difluorophenylboronic acid, of which I will use the abbreviation $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is particularly valuable in the field of organic synthesis due to its ability to serve as a key intermediate in the formation of complex organic molecules.In chemical synthesis, $name$ is often utilized as a boronic acid derivative for cross-coupling reactions, a powerful tool for forming carbon-carbon and carbon-heteroatom bonds. By incorporating $name$ into a synthetic pathway, chemists can efficiently introduce the 2,3-difluorophenyl group into target molecules while harnessing the reactivity of the boronic acid moiety.Moreover, the t-butyldimethylsilyloxy protecting group on the phenyl ring of $name$ provides an additional level of control over the reactivity of the compound. This protecting group can be selectively removed under mild conditions, allowing for further functionalization of the molecule as needed in the synthesis process.Overall, the application of 5-(t-Butyldimethylsilyloxy)-2,3-difluorophenylboronic acid in chemical synthesis enables chemists to access diverse and structurally intricate compounds with strategic precision.