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AD93600

852227-90-8 | 4-Pyrrolidinophenylboronic acid, pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $19.00 $13.00 -   +
250mg 95% in stock $28.00 $19.00 -   +
1g 95% in stock $29.00 $21.00 -   +
5g 95% in stock $129.00 $91.00 -   +
10g 95% in stock $248.00 $174.00 -   +

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*All prices are in USD.

Description
Catalog Number: AD93600
Chemical Name: 4-Pyrrolidinophenylboronic acid, pinacol ester
CAS Number: 852227-90-8
Molecular Formula: C16H24BNO2
Molecular Weight: 273.17826
MDL Number: MFCD08060504
SMILES: CC1(C)OB(OC1(C)C)c1ccc(cc1)N1CCCC1

 

Computed Properties
Complexity: 328  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 20  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine is a versatile compound widely used in chemical synthesis as a key building block. Due to its unique structure containing boron and pyrrolidine moieties, this compound plays a crucial role in various synthetic processes such as cross-coupling reactions, asymmetric catalysis, and heterocycle formation.In cross-coupling reactions, 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine acts as a valuable boronic ester derivative, enabling the formation of carbon-carbon bonds under mild reaction conditions. This facilitates the synthesis of complex organic molecules with high efficiency and selectivity.Furthermore, in asymmetric catalysis, this compound can serve as a chiral ligand or organocatalyst, aiding in the synthesis of enantiomerically pure compounds. Its ability to control stereochemistry during bond formation makes it a crucial component in the development of pharmaceuticals, agrochemicals, and other fine chemicals.Additionally, 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine is utilized in the construction of heterocycles, particularly in the synthesis of bioactive compounds and functional materials. Its diverse reactivity and compatibility with various functional groups make it a valuable tool for expanding the chemical space and accessing novel molecular architectures.Overall, the unique properties and reactivity of 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyrrolidine make it an indispensable component in modern chemical synthesis, enabling the efficient and precise construction of complex organic molecules with diverse applications.
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