1072946-54-3 | 3-(2-(Piperidin-1-yl)ethylcarbamoyl)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	96%	in stock	$56.00	$39.00
250mg	96%	in stock	$95.00	$66.00
1g	96%	in stock	$248.00	$173.00
5g	96%	in stock	$835.00	$584.00
25g	96%	in stock	$2,887.00	$2,021.00

Description

• Catalog Number: AD68730
• Chemical Name: 3-(2-(Piperidin-1-yl)ethylcarbamoyl)phenylboronic acid
• CAS Number: 1072946-54-3
• Molecular Formula: C14H21BN2O3
• Molecular Weight: 276.1391
• MDL Number: MFCD11053842
• SMILES: O=C(c1cccc(c1)B(O)O)NCCN1CCCCC1

Computed Properties

• Complexity: 309
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 20
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 5

Upstream Synthesis Route

The compound (3-((2-(piperidin-1-yl)ethyl)carbamoyl)phenyl)boronic acid, also known as $name$, is a versatile building block in chemical synthesis due to its unique structure and reactivity. This molecule is commonly used in Suzuki-Miyaura cross-coupling reactions, where it serves as a boronate ester partner to facilitate the formation of carbon-carbon bonds.In organic synthesis, $name$ can be employed as a key intermediate in the preparation of various biologically active compounds, pharmaceuticals, and materials. Its boronic acid functionality allows for selective transformations, enabling the introduction of the phenyl group into complex molecular frameworks. Additionally, the piperidine moiety in $name$ provides a handle for further derivatization, making it a valuable tool for designing novel molecules with desired properties.Overall, the application of (3-((2-(piperidin-1-yl)ethyl)carbamoyl)phenyl)boronic acid in chemical synthesis offers a strategic approach to construct diverse molecular architectures and enhance the synthetic efficiency of complex organic molecules.