1218790-11-4 | 5-(Benzyloxycarbonylamino)pyridine-3-boronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	96%	in stock	$63.00	$44.00
250mg	96%	in stock	$89.00	$62.00
1g	96%	in stock	$249.00	$175.00
5g	96%	in stock	$758.00	$531.00
10g	96%	in stock	$1,317.00	$922.00
25g	96%	in stock	$2,623.00	$1,836.00

Description

• Catalog Number: AA54518
• Chemical Name: 5-(Benzyloxycarbonylamino)pyridine-3-boronic acid, pinacol ester
• CAS Number: 1218790-11-4
• Molecular Formula: C19H23BN2O4
• Molecular Weight: 354.2079
• MDL Number: MFCD13195763
• SMILES: O=C(Nc1cncc(c1)B1OC(C(O1)(C)C)(C)C)OCc1ccccc1

Computed Properties

• Complexity: 478
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 26
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 5

Upstream Synthesis Route

Benzyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)carbamate is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role as a key building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure allows for selective functionalization at specific positions, enabling the synthesis of complex molecules with high efficiency and precision. In organic synthesis, Benzyl (5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)carbamate acts as a valuable reagent for cross-coupling reactions, facilitating the construction of carbon-carbon and carbon-heteroatom bonds. Additionally, it serves as a protecting group for sensitive functional groups, aiding in the synthesis of intricate organic compounds. This compound's widespread applicability and versatility make it an indispensable tool for chemists working in various research fields.