1188405-87-9 | 1-(t-Butoxycarbonyl)pyrazole-4-boronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$7.00	$5.00
1g	98%	in stock	$19.00	$14.00
5g	98%	in stock	$39.00	$28.00
10g	98%	in stock	$74.00	$52.00
25g	98%	in stock	$184.00	$129.00

Description

• Catalog Number: AE10013
• Chemical Name: 1-(t-Butoxycarbonyl)pyrazole-4-boronic acid
• CAS Number: 1188405-87-9
• Molecular Formula: C8H13BN2O4
• Molecular Weight: 212.0108
• MDL Number: MFCD09951915
• SMILES: OB(c1cnn(c1)C(=O)OC(C)(C)C)O

Computed Properties

• Complexity: 241
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3

Upstream Synthesis Route

The (1-(tert-Butoxycarbonyl)-1H-pyrazol-4-yl)boronic acid is a versatile compound used in chemical synthesis as a boronic acid derivative. This compound is commonly employed as a key building block in organic synthesis due to its unique reactivity and stability.One of the primary applications of (1-(tert-Butoxycarbonyl)-1H-pyrazol-4-yl)boronic acid is as a valuable reagent in Suzuki-Miyaura cross-coupling reactions. This reaction is widely utilized in the formation of carbon-carbon bonds, allowing for the synthesis of complex organic molecules. The boronic acid functionality in this compound facilitates the coupling with various organic electrophiles, enabling the construction of diverse chemical structures.Moreover, (1-(tert-Butoxycarbonyl)-1H-pyrazol-4-yl)boronic acid can also serve as a precursor for the introduction of functional groups in organic molecules. By selectively modifying the boronic acid group, chemists can introduce specific substituents or motifs into target molecules, enhancing their properties or biological activities. This versatility makes (1-(tert-Butoxycarbonyl)-1H-pyrazol-4-yl)boronic acid a valuable tool in the toolbox of synthetic chemists seeking to access a wide range of organic compounds for various applications.