496786-98-2 | 2-(4-BOC-Piperazino)pyridine-5-boronic acid, pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$10.00	$7.00
5g	97%	in stock	$38.00	$27.00
10g	97%	in stock	$67.00	$47.00
25g	97%	in stock	$153.00	$108.00
50g	97%	in stock	$266.00	$187.00
100g	97%	in stock	$516.00	$362.00

Description

• Catalog Number: AD25611
• Chemical Name: 2-(4-BOC-Piperazino)pyridine-5-boronic acid, pinacol ester
• CAS Number: 496786-98-2
• Molecular Formula: C20H32BN3O4
• Molecular Weight: 389.2968
• MDL Number: MFCD04039875
• SMILES: O=C(N1CCN(CC1)c1ccc(cn1)B1OC(C(O1)(C)C)(C)C)OC(C)(C)C

Computed Properties

• Complexity: 554
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 28
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4

Upstream Synthesis Route

The tert-Butyl 4-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)piperazine-1-carboxylate is a versatile compound frequently utilized in chemical synthesis for its unique structural properties and reactivity. Its application in organic synthesis primarily involves its use as a key building block or intermediate in the formation of complex molecules and pharmaceutical compounds. By serving as a functional group that can undergo various chemical transformations, this compound enables the synthesis of diverse structures with potential biological activities or material properties. In particular, its boron-containing moiety can participate in key bond-forming reactions, such as Suzuki-Miyaura cross-coupling, which are essential in the construction of intricate molecular frameworks. This compound's presence in the synthetic toolbox allows chemists to access a wide range of novel compounds and facilitates the exploration of new chemical reactivity pathways in the pursuit of developing innovative materials and bioactive molecules.