1192548-08-5 | 2-Fluoro-3-methylphenylboronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$15.00	$10.00
250mg	97%	in stock	$18.00	$12.00
1g	97%	in stock	$32.00	$22.00
5g	97%	in stock	$40.00	$28.00

Description

• Catalog Number: AE20137
• Chemical Name: 2-Fluoro-3-methylphenylboronic acid, pinacol ester
• CAS Number: 1192548-08-5
• Molecular Formula: C13H18BFO2
• Molecular Weight: 236.0902
• MDL Number: MFCD18384075
• SMILES: Cc1cccc(c1F)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 277
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1

Upstream Synthesis Route

2-(2-Fluoro-3-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a valuable reagent widely used in chemical synthesis for its unique properties. This compound, commonly referred to as $name$, serves as a versatile building block in various organic reactions. It plays a crucial role in cross-coupling reactions, such as Suzuki-Miyaura coupling, where it acts as a boron source for the formation of carbon-carbon bonds.Furthermore, $name$ is essential in the production of functionalized molecules and pharmaceutical intermediates. Its structure allows for efficient substitution reactions, enabling the synthesis of complex organic compounds with precision and high yield. This reagent is particularly valuable in the pharmaceutical industry for the creation of drug candidates and fine chemicals.In addition to its application in cross-coupling reactions, $name$ finds use in the preparation of advanced materials, agrochemicals, and polymers. Its stability and reactivity make it a dependable tool for synthetic chemists seeking to access a diverse range of chemical products. By incorporating $name$ into their synthetic pathways, researchers can expedite their work and achieve desired chemical transformations with ease.