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Home  > Chemistry  > Heterocyclic Building Blocks  > Piperazines  > 3-(4-Methylpiperazin-1-ylsulfonyl)phenylboronic acid pinacol ester

AE12922

1033743-79-1 | 3-(4-Methylpiperazin-1-ylsulfonyl)phenylboronic acid pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $56.00 $39.00 -   +
250mg 95% in stock $92.00 $64.00 -   +
1g 95% in stock $246.00 $172.00 -   +
5g 95% in stock $758.00 $531.00 -   +
10g 95% in stock $1,317.00 $922.00 -   +

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*All prices are in USD.

Description
Catalog Number: AE12922
Chemical Name: 3-(4-Methylpiperazin-1-ylsulfonyl)phenylboronic acid pinacol ester
CAS Number: 1033743-79-1
Molecular Formula: C17H27BN2O4S
Molecular Weight: 366.2833
MDL Number: MFCD19288884
SMILES: CN1CCN(CC1)S(=O)(=O)c1cccc(c1)B1OC(C(O1)(C)C)(C)C

 

Computed Properties
Complexity: 566  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 25  
Hydrogen Bond Acceptor Count: 6  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route
  • 3-(4-Methylpiperazin-1-ylsulfonyl)phenylboronic acid pinacol ester is a versatile compound widely utilized in chemical synthesis for its unique properties. This compound serves as a valuable building block in organic chemistry, particularly in the development of pharmaceuticals and agrochemicals. Its boronic acid functionality can form stable covalent bonds with various organic molecules, making it a valuable tool in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful method for the formation of carbon-carbon bonds, allowing for the synthesis of complex molecular structures with high efficiency and selectivity. Additionally, the presence of the pinacol ester group provides stability and solubility to the compound, facilitating its incorporation into diverse synthetic pathways. Overall, 3-(4-Methylpiperazin-1-ylsulfonyl)phenylboronic acid pinacol ester plays a crucial role in modern organic synthesis by enabling the construction of novel chemical entities with potential applications in drug discovery and material science.
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