logo
Home  > Chemistry  > Organometallic Reagents  > Organoboron  > 4-Chloro-2-fluoro-5-methylphenylboronic acid, pinacol ester

AB59043

1126320-27-1 | 4-Chloro-2-fluoro-5-methylphenylboronic acid, pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $325.00 $228.00 -   +
1g 98% in stock $791.00 $554.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB59043
Chemical Name: 4-Chloro-2-fluoro-5-methylphenylboronic acid, pinacol ester
CAS Number: 1126320-27-1
Molecular Formula: C13H17BClFO2
Molecular Weight: 270.5353
MDL Number: MFCD11855985
SMILES: CC1(C)OB(OC1(C)C)c1cc(C)c(cc1F)Cl

 

Computed Properties
Complexity: 308  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 18  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • 2-(4-Chloro-2-fluoro-5-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile reagent widely utilized in modern chemical synthesis processes. As a boronic ester, it serves as a key building block for the synthesis of various biologically active compounds, pharmaceuticals, agrochemicals, and materials.This compound plays a crucial role in Suziki-Miyaura cross-coupling reactions, allowing for the efficient formation of carbon-carbon bonds under mild reaction conditions. By introducing this boronic ester into the reaction mixture, chemists can selectively modulate the regioselectivity and stereochemistry of the resulting products, enabling the synthesis of complex molecular structures with high efficiency.Moreover, 2-(4-Chloro-2-fluoro-5-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is valued for its stability and compatibility with a wide range of functional groups, making it a valuable tool for chemists seeking to streamline their synthetic routes and enhance the overall yield and purity of their target compounds.
FEATURED PRODUCTS