logo
Home  > Chemistry  > Organic Building Blocks  > Esters  > 4-(t-Butoxycarbonyl)-5-chloro-2-fluorophenylboronic acid, pinacol ester

AA54558

1218790-25-0 | 4-(t-Butoxycarbonyl)-5-chloro-2-fluorophenylboronic acid, pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
250mg 96% in stock $123.00 $86.00 -   +
1g 96% in stock $249.00 $175.00 -   +
5g 96% in stock $945.00 $661.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA54558
Chemical Name: 4-(t-Butoxycarbonyl)-5-chloro-2-fluorophenylboronic acid, pinacol ester
CAS Number: 1218790-25-0
Molecular Formula: C17H23BClFO4
Molecular Weight: 356.6245
MDL Number: MFCD15143607
SMILES: Fc1cc(c(cc1B1OC(C(O1)(C)C)(C)C)Cl)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 476  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 24  
Hydrogen Bond Acceptor Count: 5  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • The tert-Butyl 2-chloro-5-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate compound plays a vital role in chemical synthesis as a versatile building block and reagent. This specialized compound is frequently employed in cross-coupling reactions, a key strategy in organic synthesis for forming carbon-carbon bonds. By utilizing tert-Butyl 2-chloro-5-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate, chemists can efficiently introduce the essential 2-chloro-5-fluoro-4-benzoate moiety into complex molecular structures. Additionally, the unique boron-containing functional group in this compound enables selective transformations and further diversification of chemical compounds, making it a valuable tool for researchers in the field of chemical synthesis.
FEATURED PRODUCTS