1221589-79-2 | 2,2'-(4,6-Dichloro-5-methoxy-1,3-phenylene)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)

Availability
Typically In Stock

Description

• Catalog Number: AX07255
• Chemical Name: 2,2'-(4,6-Dichloro-5-methoxy-1,3-phenylene)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)
• CAS Number: 1221589-79-2
• Molecular Formula: C19H28B2Cl2O5
• Molecular Weight: 428.9506
• MDL Number: MFCD29917023
• SMILES: COc1c(Cl)c(cc(c1Cl)B1OC(C(O1)(C)C)(C)C)B1OC(C(O1)(C)C)(C)C

Upstream Synthesis Route

2-[2,4-dichloro-3-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile compound widely used in chemical synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. It serves as a valuable building block in the construction of complex organic molecules due to its unique reactivity and stability. This compound is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron source to introduce the desired aryl group onto another organic molecule. Additionally, it finds application in the synthesis of pharmaceuticals, agrochemicals, and materials due to its ability to facilitate selective and efficient bond formation processes. Its controlled reactivity and compatibility with a variety of functional groups make it an essential tool in the toolbox of synthetic chemists striving to create novel compounds with tailored properties.