1073354-73-0 | 6-[Cyclohexyl(methyl)amino]pyridine-3-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$105.00	$74.00
1g	95%	in stock	$265.00	$186.00

Description

• Catalog Number: AB77252
• Chemical Name: 6-[Cyclohexyl(methyl)amino]pyridine-3-boronic acid pinacol ester
• CAS Number: 1073354-73-0
• Molecular Formula: C18H29BN2O2
• Molecular Weight: 316.2461
• MDL Number: MFCD09027071
• SMILES: CN(c1ccc(cn1)B1OC(C(O1)(C)C)(C)C)C1CCCCC1

Computed Properties

• Complexity: 394
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 23
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3

Upstream Synthesis Route

N-Cyclohexyl-N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine is a versatile compound widely used in chemical synthesis as a key building block in the preparation of various organic molecules. This compound serves as an essential reagent in the Suzuki-Miyaura cross-coupling reaction, a fundamental process in modern organic synthesis for creating carbon-carbon bonds.In the context of chemical synthesis, this compound plays a crucial role as a ligand in palladium-catalyzed coupling reactions, enabling the selective formation of complex organic structures with high efficiency. Its unique structure containing a boron atom coordinated to a cyclic amine moiety enhances the reactivity and selectivity of the cross-coupling reactions, making it a valuable tool for the synthesis of pharmaceuticals, agrochemicals, and advanced materials.Furthermore, the N-Cyclohexyl-N-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine scaffold can be modified through functional group transformations to introduce diverse chemical functionalities into the final products. This flexibility and reactivity make it a versatile and indispensable component in the toolbox of synthetic chemists for the construction of complex molecular architectures with high precision and control.