1900755-49-8 | (1-Tritylimidazol-4-yl)boronic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$199.00	$139.00
250mg	95%	in stock	$289.00	$202.00

Description

• Catalog Number: AY09828
• Chemical Name: (1-Tritylimidazol-4-yl)boronic acid
• CAS Number: 1900755-49-8
• Molecular Formula: C22H19BN2O2
• Molecular Weight: 354.2095
• MDL Number: MFCD10696629
• SMILES: OB(c1ncn(c1)C(c1ccccc1)(c1ccccc1)c1ccccc1)O

Computed Properties

• Complexity: 412
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 27
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5

Upstream Synthesis Route

The (1-Tritylimidazol-4-yl)boronic acid is a versatile chemical compound widely utilized in organic synthesis due to its unique reactivity and functional group compatibility. It serves as a key building block in the construction of complex molecular structures, particularly in the field of medicinal chemistry and material science.In chemical synthesis, (1-Tritylimidazol-4-yl)boronic acid acts as a powerful boron source for Suzuki-Miyaura cross-coupling reactions. This classic coupling reaction involves the formation of carbon-carbon bonds under mild reaction conditions, making it invaluable for the assembly of biaryl compounds, which are prevalent in pharmaceuticals, agrochemicals, and materials science applications.The boronic acid functionality in (1-Tritylimidazol-4-yl)boronic acid is crucial for its reactivity in organic transformations. By easily forming stable boronate complexes with aryl halides or pseudohalides, this compound can participate in selective coupling reactions to create new carbon-carbon bonds with high efficiency and selectivity. This feature makes it an essential tool for the streamlined synthesis of diverse organic molecules with tailored properties.Moreover, (1-Tritylimidazol-4-yl)boronic acid's stability under a wide range of reaction conditions and its compatibility with various functional groups further enhance its utility in chemical synthesis. Its ability to undergo oxidative addition and reductive elimination processes enables the smooth construction of complex molecular architectures, making it a valuable reagent in the hands of synthetic chemists striving to access novel compounds for a myriad of applications.