1025735-46-9 | 3-(3,5-Dimethyl-1h-pyrazol-1-yl)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$106.00	$75.00
1g	95%	in stock	$259.00	$181.00
5g	95%	in stock	$837.00	$586.00
10g	95%	in stock	$1,443.00	$1,010.00
25g	95%	in stock	$2,858.00	$2,000.00

Description

• Catalog Number: AA09883
• Chemical Name: 3-(3,5-Dimethyl-1h-pyrazol-1-yl)phenylboronic acid
• CAS Number: 1025735-46-9
• Molecular Formula: C11H13BN2O2
• Molecular Weight: 216.0441
• MDL Number: MFCD08572151
• SMILES: Cc1nn(c(c1)C)c1cccc(c1)B(O)O

Computed Properties

• Complexity: 240
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2

Upstream Synthesis Route

3-(3,5-dimethyl-1H-pyrazol-1-yl)phenylboronic acid is a versatile compound widely utilized in chemical synthesis for its exceptional reactivity and functionality. This unique molecule acts as a key building block in various organic reactions, particularly in the field of organic and medicinal chemistry.One of the primary applications of 3-(3,5-dimethyl-1H-pyrazol-1-yl)phenylboronic acid is its use as a ligand in transition metal-catalyzed cross-coupling reactions. The boronic acid functionality allows for facile Suzuki-Miyaura coupling reactions, enabling the synthesis of complex biaryl compounds. This compound is often employed in the preparation of pharmaceutical intermediates and functional materials due to its ability to facilitate selective carbon-carbon bond formations.Moreover, 3-(3,5-dimethyl-1H-pyrazol-1-yl)phenylboronic acid serves as a valuable tool in the construction of molecular scaffolds with specific stereochemical properties. Its unique structure and reactivity make it an indispensable component in the synthesis of heterocyclic compounds and bioactive molecules. Researchers and chemists leverage the versatility of this compound to streamline the synthesis of diverse organic molecules with tailored properties and functionalities.