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490035-82-0

Methyl 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoate

Catalog#: AR00E80O  |   CAS#: 490035-82-0  |   MDL#: MFCD16996366  |   MF: C16H23BO4  |   MW: 290.16241999999994

Packsize Purity Price Availability Quantity
100mg 98% $24.00 Global Stock Buy Now Add To Cart
250mg 98% $41.00 Global Stock Buy Now Add To Cart
1g 98% $104.00 Global Stock Buy Now Add To Cart
5g 98% $398.00 Global Stock Buy Now Add To Cart
10g 98% $741.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00E80O
Chemical Name Methyl 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoate
CAS Number 490035-82-0
Molecular Formula C16H23BO4
Molecular Weight 290.16241999999994
MDL Number MFCD16996366
SMILES COC(=O)CCc1ccc(cc1)B1OC(C(O1)(C)C)(C)C

Application of Methyl 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoate in Chemical Synthesis:Methyl 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoate serves as a valuable building block in chemical synthesis due to its unique structure and reactivity. This compound is commonly utilized as a key intermediate in the preparation of various functionalized organic molecules.In organic synthesis, Methyl 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoate is frequently employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to introduce diverse functional groups onto the phenyl ring. Its boron-containing moiety makes it a versatile substrate for transition metal-catalyzed transformations, allowing for the construction of complex molecular architectures with high efficiency and selectivity.Furthermore, the ester functionality of this compound enables further derivatization through various chemical reactions, such as ester hydrolysis, reduction, or transesterification, providing access to a wide range of structurally diverse compounds for various applications in medicinal chemistry, materials science, and agrochemicals.Overall, Methyl 3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoate plays a crucial role in modern synthetic methodologies by serving as a versatile synthon for the construction of complex organic molecules with tailored properties and functionalities.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302
Precautionary Statements P280-P305+P351+P338
Class -
Packing Group -

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