1072951-59-7 | 3,5-Diiodo-2-methoxyphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$42.00	$30.00
1g	97%	in stock	$66.00	$47.00

Description

• Catalog Number: AB63942
• Chemical Name: 3,5-Diiodo-2-methoxyphenylboronic acid
• CAS Number: 1072951-59-7
• Molecular Formula: C7H7BI2O3
• Molecular Weight: 403.7486
• MDL Number: MFCD08457647
• SMILES: COc1c(I)cc(cc1B(O)O)I

Computed Properties

• Complexity: 170
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2

Upstream Synthesis Route

The (3,5-Diiodo-2-methoxyphenyl)boronic acid, commonly referred to as $name$, is a versatile compound widely utilized in chemical synthesis. Due to its unique structure and reactivity, this boronic acid derivative serves as a valuable building block in the preparation of pharmaceuticals, agrochemicals, and various advanced materials. In organic synthesis, $name$ acts as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of C-C bonds through the coupling of aryl halides with various nucleophiles. This methodology has been widely employed in the synthesis of complex molecules, including natural products and drug candidates. Additionally, the presence of electron-withdrawing iodine substituents in $name$ enhances its stability and reactivity in challenging synthetic transformations.Moreover, the methoxy group in the molecular structure of $name$ provides a directing effect in transition metal-catalyzed reactions, facilitating selective functionalization at specific positions within aromatic molecules. This feature proves especially useful in the selective modification of complex drug-like scaffolds and the construction of novel molecular architectures.Overall, the (3,5-Diiodo-2-methoxyphenyl)boronic acid plays a crucial role in modern organic synthesis, enabling chemists to access a diverse array of functionalized compounds with high efficiency and selectivity. Its broad utility and compatibility with various synthetic methodologies make it a valuable tool for researchers working in medicinal chemistry, materials science, and other fields requiring intricate molecular design and synthesis capabilities.