1072951-55-3 | 5-Trifluoromethylquinoline-8-boronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	96%	in stock	$356.00	$249.00
1g	96%	in stock	$869.00	$608.00
5g	96%	in stock	$3,434.00	$2,404.00

Description

• Catalog Number: AB55231
• Chemical Name: 5-Trifluoromethylquinoline-8-boronic acid
• CAS Number: 1072951-55-3
• Molecular Formula: C10H7BF3NO2
• Molecular Weight: 240.9743
• MDL Number: MFCD11504856
• SMILES: OB(c1ccc(c2c1nccc2)C(F)(F)F)O

Computed Properties

• Complexity: 275
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1

Upstream Synthesis Route

$Name$ is a versatile chemical compound that finds widespread application in chemical synthesis procedures, particularly in the realm of organic synthesis. This compound, also known as (5-(Trifluoromethyl)quinolin-8-yl)boronic acid, is highly valued for its unique chemical properties and reactivity in various reactions.In chemical synthesis, (5-(Trifluoromethyl)quinolin-8-yl)boronic acid serves as a valuable building block for creating complex organic molecules through cross-coupling reactions. It is commonly used in Suzuki-Miyaura coupling reactions, where it acts as a boron source to form carbon-carbon bonds with aryl halides or pseudohalides. This process allows for the efficient and precise assembly of organic molecules with diverse structures and functionalities.Additionally, (5-(Trifluoromethyl)quinolin-8-yl)boronic acid can be utilized in transition metal-catalyzed reactions to introduce the trifluoromethyl group into organic molecules. This fluorinated motif is of great interest in medicinal chemistry and material science due to its unique physicochemical properties that can enhance the biological activity or material properties of the resulting compounds.Overall, the application of (5-(Trifluoromethyl)quinolin-8-yl)boronic acid in chemical synthesis offers chemists a powerful tool for constructing complex organic molecules with specific functionalities, making it a valuable asset in the toolkit of synthetic chemists.