1015242-08-6 | 2-Piperidinopyrimidine-5-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$42.00	$30.00
1g	98%	in stock	$111.00	$78.00
5g	98%	in stock	$411.00	$288.00

Description

• Catalog Number: AA05897
• Chemical Name: 2-Piperidinopyrimidine-5-boronic acid pinacol ester
• CAS Number: 1015242-08-6
• Molecular Formula: C15H24BN3O2
• Molecular Weight: 289.181
• MDL Number: MFCD07368250
• SMILES: CC1(C)OB(OC1(C)C)c1cnc(nc1)N1CCCCC1

Computed Properties

• Complexity: 348
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 21
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2

Upstream Synthesis Route

The compound $name$ serves as a versatile building block in chemical synthesis due to its unique structure and reactivity. It is commonly used as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, $name$ can be employed in Suzuki-Miyaura cross-coupling reactions to introduce the pyrimidine moiety into more complex molecules. Additionally, the boronic ester functionality of $name$ allows for further functionalization through various transformations such as oxidation, reduction, and substitution reactions, enabling the modification of its chemical properties.Furthermore, the presence of the dihydropyridine group in $name$ offers the potential for bioisosteric replacement in medicinal chemistry, making it a valuable scaffold for the design of novel drug candidates. Overall, the application of 2-(3,4-Dihydropyridin-1(2H)-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine in chemical synthesis demonstrates its significance in the creation of complex molecules with diverse functionalities and potential pharmacological activities.