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AA20272

1150561-77-5 | 2-(Methoxycarbonyl)ethylboronic acid, pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $7.00 $5.00 -   +
1g 98% in stock $20.00 $14.00 -   +
2500mg 98% in stock $43.00 $31.00 -   +
5g 98% in stock $59.00 $42.00 -   +
10g 98% in stock $95.00 $67.00 -   +
25g 98% in stock $226.00 $159.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA20272
Chemical Name: 2-(Methoxycarbonyl)ethylboronic acid, pinacol ester
CAS Number: 1150561-77-5
Molecular Formula: C10H19BO4
Molecular Weight: 214.06645999999995
MDL Number: MFCD10700159
SMILES: COC(=O)CCB1OC(C(O1)(C)C)(C)C

 

Computed Properties
Complexity: 234  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 4  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • Methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate is a versatile compound widely used in chemical synthesis due to its unique reactivity and functional group compatibility. It serves as a valuable building block in organic chemistry, particularly in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.This compound is commonly employed as a key intermediate in Suzuki-Miyaura cross-coupling reactions, a powerful tool in modern organic synthesis for forming carbon-carbon bonds. By utilizing Methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate as a boronic acid ester, chemists can efficiently introduce various functional groups onto aromatic and aliphatic substrates under mild reaction conditions.Furthermore, the compatibility of this compound with a variety of reaction partners makes it a valuable tool for the construction of complex molecular structures. Its stability and ease of handling make it a preferred choice for synthetic chemists looking to streamline their processes and achieve high yields of desired products.In summary, Methyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propanoate is an essential building block in chemical synthesis, offering a range of applications in the efficient formation of carbon-carbon bonds and the synthesis of diverse organic molecules.
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