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Home  > 3-(t-Butyldimethylsilyloxy)-5-(methoxycarbonyl)phenylboronic acid, pinacol ester

AA54492

1218789-68-4 | 3-(t-Butyldimethylsilyloxy)-5-(methoxycarbonyl)phenylboronic acid, pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $99.00 $69.00 -   +
1g 98% in stock $251.00 $176.00 -   +
5g 98% in stock $869.00 $608.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA54492
Chemical Name: 3-(t-Butyldimethylsilyloxy)-5-(methoxycarbonyl)phenylboronic acid, pinacol ester
CAS Number: 1218789-68-4
Molecular Formula: C20H33BO5Si
Molecular Weight: 392.3695199999999
MDL Number: MFCD12546599
SMILES: COC(=O)c1cc(cc(c1)B1OC(C(O1)(C)C)(C)C)O[Si](C(C)(C)C)(C)C

 

Upstream Synthesis Route
  • Methyl 3-((tert-butyldimethylsilyl)oxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is a versatile compound utilized in organic chemical synthesis as a key building block. This compound is commonly employed in the protection of hydroxyl groups in various organic molecules, particularly in the synthesis of complex natural products and pharmaceutical compounds. The tert-butyldimethylsilyl (TBS) protecting group attached to the hydroxyl group provides stability during various chemical reactions, allowing selective deprotection at a later stage. Additionally, the boronate ester functionality in this compound serves as a useful handle for cross-coupling reactions, enabling the introduction of diverse functional groups or moieties in a controlled manner. Overall, the strategic incorporation of Methyl 3-((tert-butyldimethylsilyl)oxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate in chemical synthesis facilitates the efficient construction of complex molecular architectures with high precision and selectivity.
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