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Home  > (E)-2-(2-Ethoxycarbonylvinyl)phenylboronic acid, pinacol ester

AB55352

1132669-74-9 | (E)-2-(2-Ethoxycarbonylvinyl)phenylboronic acid, pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $43.00 $30.00 -   +
250mg 95% in stock $70.00 $49.00 -   +
1g 95% in stock $184.00 $129.00 -   +
5g 95% in stock $912.00 $639.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB55352
Chemical Name: (E)-2-(2-Ethoxycarbonylvinyl)phenylboronic acid, pinacol ester
CAS Number: 1132669-74-9
Molecular Formula: C17H23BO4
Molecular Weight: 302.1731
MDL Number: MFCD16036137
SMILES: CCOC(=O)/C=C/c1ccccc1B1OC(C(O1)(C)C)(C)C

 

Computed Properties
Complexity: 414  
Covalently-Bonded Unit Count: 1  
Defined Bond Stereocenter Count: 1  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 4  
Rotatable Bond Count: 5  

 

 

Upstream Synthesis Route
  • The compound (E)-Ethyl 3-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acrylate is widely utilized in chemical synthesis as a versatile building block. With its unique structure containing both the boronate and acrylate functional groups, this compound serves as a key intermediate in the production of various organic compounds. Its application lies in the realm of organic synthesis reactions, particularly in cross-coupling processes where the boronate group acts as a reactive site for coupling with different electrophiles. This compound plays a crucial role in the formation of carbon-carbon bonds, enabling the creation of intricate organic molecules with diverse functionalities. Furthermore, its presence enhances the reactivity and selectivity of the overall synthesis, making it a valuable tool for chemists engaged in complex molecule construction.
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