1165936-00-4 | 2-Fluoro-3-methoxyphenylboronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$25.00	$17.00
5g	98%	in stock	$62.00	$43.00
10g	98%	in stock	$105.00	$74.00
25g	98%	in stock	$201.00	$141.00
100g	98%	in stock	$572.00	$400.00

Description

• Catalog Number: AA16432
• Chemical Name: 2-Fluoro-3-methoxyphenylboronic acid pinacol ester
• CAS Number: 1165936-00-4
• Molecular Formula: C13H18BFO3
• Molecular Weight: 252.0896
• MDL Number: MFCD16618962
• SMILES: COc1cccc(c1F)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 293
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2

Upstream Synthesis Route

2-(2-Fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile chemical compound that finds wide application in chemical synthesis processes. Specifically, this compound serves as a valuable boronic ester reagent that is utilized in various cross-coupling reactions, particularly in the field of organic chemistry.In chemical synthesis, 2-(2-Fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane acts as a key component in reactions such as Suzuki-Miyaura coupling, which involves the cross-coupling of organoboron compounds with organic halides or pseudohalides. This compound is particularly useful in C-C bond formation, enabling the creation of complex organic molecules with high efficiency and selectivity.The unique structure of 2-(2-Fluoro-3-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane provides it with excellent reactivity and compatibility with a wide range of substrates, making it a valuable tool for the synthesis of pharmaceuticals, agrochemicals, materials, and other important organic compounds. Its ease of use and reliability make it a preferred choice for chemists working in the field of organic synthesis.