1002129-33-0 | 6-(Piperidin-1-yl)pyridine-3-boronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$106.00	$75.00
1g	98%	in stock	$171.00	$120.00
5g	98%	in stock	$636.00	$445.00
25g	98%	in stock	$2,345.00	$1,642.00

Description

• Catalog Number: AA01429
• Chemical Name: 6-(Piperidin-1-yl)pyridine-3-boronic acid
• CAS Number: 1002129-33-0
• Molecular Formula: C10H15BN2O2
• Molecular Weight: 206.0493
• MDL Number: MFCD06801705
• SMILES: OB(c1ccc(nc1)N1CCCCC1)O

Computed Properties

• Complexity: 198
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2

Upstream Synthesis Route

(6-(Piperidin-1-yl)pyridin-3-yl)boronic acid is a versatile compound that plays a crucial role in chemical synthesis, particularly in the field of organic chemistry. This specific boronic acid derivative is known for its unique ability to act as a key building block in the construction of complex molecular structures.One of the primary applications of (6-(Piperidin-1-yl)pyridin-3-yl)boronic acid lies in its utility as a ligand in transition metal-catalyzed cross-coupling reactions. These reactions, such as the Suzuki-Miyaura coupling, allow for the selective formation of carbon-carbon bonds between organic substrates, leading to the synthesis of various biaryl compounds. The boronic acid moiety in this compound serves as an essential component in facilitating these coupling reactions by forming stable complexes with transition metals.Furthermore, (6-(Piperidin-1-yl)pyridin-3-yl)boronic acid can also be employed in the preparation of diverse pharmaceuticals, agrochemicals, and materials due to its ability to undergo selective transformations in the presence of suitable catalysts. By utilizing this boronic acid derivative as a starting material, chemists can access a wide array of functionalized molecules with tailored properties and applications. Its compatibility with various reaction conditions and its high reactivity make it an indispensable tool in the synthesis of complex organic compounds with specific functionalities.