1002309-48-9 | 1-Cyclobutyl-1H-pyrazole-4-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$32.00	$23.00
5g	97%	in stock	$149.00	$105.00

Description

• Catalog Number: AA01481
• Chemical Name: 1-Cyclobutyl-1H-pyrazole-4-boronic acid pinacol ester
• CAS Number: 1002309-48-9
• Molecular Formula: C13H21BN2O2
• Molecular Weight: 248.12904000000006
• MDL Number: MFCD16659010
• SMILES: CC1(C)OB(OC1(C)C)c1cnn(c1)C1CCC1

Computed Properties

• Complexity: 315
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2

Upstream Synthesis Route

1-Cyclobutyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is a versatile compound widely used in chemical synthesis due to its unique structural properties. This compound serves as a valuable building block in the preparation of various organic molecules and materials. In particular, its boron-containing moiety offers opportunities for cross-coupling reactions, such as Suzuki-Miyaura coupling, enabling the efficient formation of carbon-carbon bonds. Additionally, the presence of the cyclobutyl and pyrazole groups in the molecule imparts specific reactivity and functionality to the compound, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and functional materials. Furthermore, the sterically hindered nature of the tetramethyl substituents on the boron atom enhances the stability and selectivity of reactions involving this compound. Overall, the strategic incorporation of 1-Cyclobutyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole in chemical synthesis allows for the efficient construction of complex molecular architectures with potential applications across various sectors of the chemical industry.