1217501-39-7 | 4-Cyclopentenylphenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$139.00	$97.00
5g	98%	in stock	$387.00	$271.00
10g	98%	in stock	$667.00	$467.00
25g	98%	in stock	$1,319.00	$923.00

Description

• Catalog Number: AA53946
• Chemical Name: 4-Cyclopentenylphenylboronic acid
• CAS Number: 1217501-39-7
• Molecular Formula: C11H13BO2
• Molecular Weight: 188.0307
• MDL Number: MFCD13195659
• SMILES: OB(c1ccc(cc1)C1=CCCC1)O

Computed Properties

• Complexity: 217
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2

Upstream Synthesis Route

B-[4-(1-Cyclopenten-1-yl)phenyl]boronic acid, also known as $name$, is a versatile chemical compound widely used in organic synthesis. It serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties.In chemical synthesis, $name$ is commonly utilized as a key reagent in Suzuki-Miyaura cross-coupling reactions. This versatile reaction allows for the formation of carbon-carbon bonds, enabling the construction of complex molecular structures with high efficiency and selectivity. The presence of a boronic acid group in $name$ facilitates its compatibility with a wide range of coupling partners, making it a valuable tool in the synthesis of biaryl compounds and heterocyclic molecules.$name$ also finds application in the preparation of functionalized organoboron compounds, which have emerged as important intermediates in modern organic synthesis. These compounds serve as valuable precursors for the introduction of functional groups such as alkyl, aryl, or heteroaryl moieties into organic molecules, expanding the chemical diversity and utility of the final products.Overall, the role of B-[4-(1-Cyclopenten-1-yl)phenyl]boronic acid in chemical synthesis is paramount, enabling chemists to access a versatile toolkit for the construction of complex molecular structures with strategic precision and synthetic efficiency.