1040377-08-9 | 1-(2-Hydroxyethyl)-1h-pyrazole-4-boronic acid pinacol ester

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$8.00	$6.00
250mg	95%	in stock	$13.00	$9.00
1g	95%	in stock	$18.00	$13.00
5g	95%	in stock	$82.00	$58.00
10g	95%	in stock	$155.00	$108.00

Description

• Catalog Number: AD68886
• Chemical Name: 1-(2-Hydroxyethyl)-1h-pyrazole-4-boronic acid pinacol ester
• CAS Number: 1040377-08-9
• Molecular Formula: C11H19BN2O3
• Molecular Weight: 238.0912
• MDL Number: MFCD12033564
• SMILES: OCCn1ncc(c1)B1OC(C(O1)(C)C)(C)C

Computed Properties

• Complexity: 270
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3

Upstream Synthesis Route

The compound 2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethanol is a versatile reagent that finds significant applications in chemical synthesis. It serves as a valuable building block in organic chemistry, particularly in the formation of complex molecules and pharmaceuticals.Due to its unique structural properties, this compound can participate in various synthetic reactions such as Suzuki-Miyaura cross-coupling reactions, which are widely utilized in the synthesis of pharmaceuticals, agrochemicals, and materials science. The boron moiety in the molecule can act as a versatile handle for further functionalization, allowing for the introduction of a wide range of substituents with high efficiency and selectivity.Furthermore, the pyrazole ring in the compound confers desirable reactivity and selectivity in various transformations, making it a valuable tool in the construction of heterocyclic scaffolds commonly found in bioactive compounds. Its ability to undergo selective transformations under mild conditions makes it an attractive option for chemists seeking to streamline synthetic routes and access complex molecular architectures.In summary, the application of 2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethanol in chemical synthesis lies in its versatility as a building block for the construction of diverse organic molecules, particularly in the synthesis of pharmaceuticals and biologically active compounds.