1217501-31-9 | 3-(5-Methyl-1,2,4-oxadiazol-3-yl)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$480.00	$336.00
1g	97%	in stock	$1,024.00	$717.00

Description

• Catalog Number: AA53953
• Chemical Name: 3-(5-Methyl-1,2,4-oxadiazol-3-yl)phenylboronic acid
• CAS Number: 1217501-31-9
• Molecular Formula: C9H9BN2O3
• Molecular Weight: 203.9904
• MDL Number: MFCD13195651
• SMILES: Cc1onc(n1)c1cccc(c1)B(O)O

Computed Properties

• Complexity: 218
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2

Upstream Synthesis Route

(3-(5-Methyl-1,2,4-oxadiazol-3-yl)phenyl)boronic acid is a versatile compound used in chemical synthesis for its ability to participate in various reactions, particularly in the field of organic chemistry. This compound serves as a valuable building block for the synthesis of biologically active molecules, pharmaceuticals, agrochemicals, and materials with specific properties.In organic synthesis, (3-(5-Methyl-1,2,4-oxadiazol-3-yl)phenyl)boronic acid plays a significant role as a boronic acid derivative. It is commonly employed in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This compound can undergo cross-coupling reactions with aryl halides or triflates in the presence of a palladium catalyst to yield substituted biaryl compounds.Additionally, (3-(5-Methyl-1,2,4-oxadiazol-3-yl)phenyl)boronic acid can participate in other transformations such as C-H activation reactions, borylation reactions, and various functional group interconversions. Its versatile reactivity and compatibility with a wide range of functional groups make it a valuable tool for synthetic chemists seeking to construct complex molecular structures efficiently.