CAS 1008139-25-0: 1,2-Oxazol-4-ylboronic acid

Description: 1,2-Oxazol-4-ylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a 1,2-oxazole ring. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and alcohols, and possessing acidic characteristics due to the boronic acid moiety. The oxazole ring contributes to its heterocyclic nature, which can influence its reactivity and interactions in various chemical environments. It is often utilized in organic synthesis, particularly in Suzuki coupling reactions, where it serves as a versatile building block for the formation of carbon-carbon bonds. Additionally, the presence of the boronic acid group allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to form reversible covalent bonds with diols. Overall, 1,2-Oxazol-4-ylboronic acid is a valuable compound in both academic and industrial chemistry settings, owing to its unique structural features and reactivity.

Synonyms:

• Isoxazole-4-boronic acid

Boronic acid, B-4-isoxazolyl-

CAS: 1008139-25-0

• Formula: C₃H₄BNO₃
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 112.8798

Isoxazole-4-boronic acid

CAS: 1008139-25-0

• Purity: 95.0%
• Color and Shape: Solid
• Molecular weight: 112.87999725341797

Isoxazole-4-boronic acid

CAS: 1008139-25-0

• Formula: C₃H₄BNO₃
• Purity: 0.97
• Color and Shape: pale yellow solid
• Molecular weight: 112.88g/mol

Isoxazole-4-boronic acid

CAS: 1008139-25-0

Isoxazole-4-boronic acid is a postulated intermediate in the synthesis of aryl bromides and aryl halides. …

• Formula: C₃H₄BNO₃
• Purity: Min. 95%
• Molecular weight: 112.88 g/mol