1032610-59-5 | 3-(Piperidin-1-ylmethyl)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$63.00	$44.00
1g	95%	in stock	$160.00	$112.00
5g	95%	in stock	$712.00	$498.00
10g	95%	in stock	$1,053.00	$737.00

Description

• Catalog Number: AE10425
• Chemical Name: 3-(Piperidin-1-ylmethyl)phenylboronic acid
• CAS Number: 1032610-59-5
• Molecular Formula: C12H18BNO2
• Molecular Weight: 219.0878200000001
• MDL Number: MFCD08060620
• SMILES: OB(c1cccc(c1)CN1CCCCC1)O

Computed Properties

• Complexity: 207
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3

Upstream Synthesis Route

The chemical compound (3-(Piperidin-1-ylmethyl)phenyl)boronic acid, also known as $name$, is a versatile reagent commonly used in chemical synthesis. Its primary application lies in the field of organic chemistry, where it serves as a valuable building block for the creation of complex molecules.One of the key roles of (3-(Piperidin-1-ylmethyl)phenyl)boronic acid is its ability to participate in Suzuki-Miyaura cross-coupling reactions. In this process, the boronic acid moiety acts as a nucleophilic partner, reacting with an electrophilic partner in the presence of a palladium catalyst to form a new carbon-carbon bond. This versatile reaction allows for the synthesis of a wide range of biaryl compounds, which are essential in the pharmaceutical, agrochemical, and materials science industries.Furthermore, (3-(Piperidin-1-ylmethyl)phenyl)boronic acid is also utilized in the construction of various organic molecules through boronate ester formation. By reacting with suitable electrophiles, the boronic acid group can undergo oxidative addition to form stable boronate esters, which can subsequently be transformed into a variety of functional groups. This functional group interconversion strategy is particularly valuable in the synthesis of pharmaceuticals and fine chemicals.Overall, the application of (3-(Piperidin-1-ylmethyl)phenyl)boronic acid in chemical synthesis enables chemists to access diverse molecular architectures efficiently and selectively, making it a valuable tool in the development of new chemical entities and molecular probes.