1015242-03-1 | 1-Benzyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$87.00	$61.00
250mg	98%	in stock	$133.00	$93.00
1g	98%	in stock	$331.00	$232.00
5g	98%	in stock	$1,275.00	$893.00

Description

• Catalog Number: AA05900
• Chemical Name: 1-Benzyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine
• CAS Number: 1015242-03-1
• Molecular Formula: C22H30BN3O2
• Molecular Weight: 379.3035
• MDL Number: MFCD06798275
• SMILES: CC1(C)OB(OC1(C)C)c1ccc(nc1)N1CCN(CC1)Cc1ccccc1

Computed Properties

• Complexity: 500
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 28
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4

Upstream Synthesis Route

1-Benzyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. This molecule serves as a valuable building block in the creation of complex organic structures due to its structural features and functional groups.In chemical synthesis, 1-Benzyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine can act as a key intermediate for the formation of various heterocyclic compounds. Its substituted pyridine and piperazine moieties enable it to participate in a range of organic transformations, including cross-coupling reactions, nucleophilic substitutions, and metal-catalyzed processes.Furthermore, the boron-containing moiety in 1-Benzyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine offers a unique handle for further functionalization and site-selective chemical modifications. This feature enhances its utility in the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties.Overall, the strategic incorporation of 1-Benzyl-4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine in chemical synthesis enables efficient access to diverse molecular scaffolds and promotes the development of novel compounds with potential applications in various fields.