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128376-64-7

Benzaldehyde, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

Catalog#: AR000YQJ  |   CAS#: 128376-64-7  |   MDL#: MFCD04972375  |   MF: C13H17BO3  |   MW: 232.0833

Packsize Purity Price Availability Quantity
1g 98% $3.00 Global Stock Buy Now Add To Cart
5g 98% $7.00 Global Stock Buy Now Add To Cart
10g 98% $13.00 Global Stock Buy Now Add To Cart
25g 98% $26.00 Global Stock Buy Now Add To Cart
100g 98% $95.00 Global Stock Buy Now Add To Cart
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Catalog Number AR000YQJ
Chemical Name Benzaldehyde, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS Number 128376-64-7
Molecular Formula C13H17BO3
Molecular Weight 232.0833
MDL Number MFCD04972375
SMILES O=Cc1ccc(cc1)B1OC(C(O1)(C)C)(C)C

4-Formylphenylboronic acid pinacol cyclic ester, also known as $name$, is a versatile compound widely used in chemical synthesis as a key building block. This unique molecule plays a crucial role in the formation of complex organic structures due to its ability to undergo various chemical reactions.In organic chemistry, $name$ is commonly utilized for the selective functionalization of aromatic compounds. Its boronic acid moiety enables it to participate in Suzuki-Miyaura cross-coupling reactions, where it serves as a nucleophilic partner to form carbon-carbon bonds. This reaction is essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.Additionally, $name$ can undergo oxidative transformations to yield aldehydes or carboxylic acids, expanding its utility in the preparation of diverse organic molecules. Its cyclic ester structure, derived from pinacol, provides stability and enhances its compatibility in various synthetic methods.Moreover, the presence of the formyl group in $name$ enables it to serve as a versatile precursor for the introduction of functional groups such as amines, alcohols, and halides through subsequent chemical modifications. This characteristic makes $name$ a valuable tool in the design of intricate molecular scaffolds.Overall, the strategic incorporation of 4-Formylphenylboronic acid pinacol cyclic ester in chemical synthesis offers chemists a powerful platform for the efficient construction of complex organic molecules with precise control over regioselectivity and functional group compatibility. Its diverse reactivity and structural features make it an indispensable component in modern synthetic methodologies.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H317
Precautionary Statements P261-P280
Class N/A
Packing Group N/A

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