1218791-32-2 | 2,6-Difluoro-4-(methoxycarbonyl)phenylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$86.00	$60.00
1g	98%	in stock	$243.00	$170.00
5g	98%	in stock	$828.00	$580.00
25g	98%	in stock	$2,879.00	$2,016.00
100g	98%	in stock	$9,487.00	$6,641.00

Description

• Catalog Number: AA54652
• Chemical Name: 2,6-Difluoro-4-(methoxycarbonyl)phenylboronic acid, pinacol ester
• CAS Number: 1218791-32-2
• Molecular Formula: C14H17BF2O4
• Molecular Weight: 298.0902
• MDL Number: MFCD12546491
• SMILES: COC(=O)c1cc(F)c(c(c1)F)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 388
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 21
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3

Upstream Synthesis Route

Methyl 3,5-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is a versatile chemical compound commonly used in chemical synthesis processes. This compound plays a significant role in modern organic chemistry, particularly in the synthesis of complex organic molecules.One of the key applications of Methyl 3,5-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is as a reagent for Suzuki-Miyaura cross-coupling reactions. In this process, the compound acts as a boronic ester, which can undergo a palladium-catalyzed coupling reaction with various aryl halides or pseudohalides. This reaction is widely used in the construction of carbon-carbon bonds, allowing for the formation of new carbon-carbon bonds in a controlled and efficient manner.Furthermore, Methyl 3,5-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate can also serve as a valuable building block for the synthesis of biologically active compounds, pharmaceutical intermediates, agrochemicals, and materials with specific properties. Its unique structural features make it a versatile precursor in the design and production of novel molecules with tailored functionalities.Overall, the application of Methyl 3,5-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate in chemical synthesis provides researchers and chemists with a powerful tool for the efficient and controlled synthesis of diverse organic compounds with potential applications in various fields of science and industry.