1-Bromo-2-naphthoic Acid: Chemical Properties and Synthesis Routes
For chemists and researchers involved in organic synthesis, a thorough understanding of chemical intermediates is paramount. 1-Bromo-2-naphthoic Acid (CAS 20717-79-7) stands out as a versatile compound, frequently employed in various synthetic pathways. Its unique structural features, including a brominated naphthalene ring coupled with a carboxylic acid functional group, dictate its chemical behavior and reactivity. This article delves into the essential chemical properties of 1-Bromo-2-naphthoic Acid and discusses common synthesis routes, providing valuable insights for professionals looking to buy this compound.
The chemical identity of 1-Bromo-2-naphthoic Acid is defined by its molecular formula C11H7BrO2 and a molecular weight of approximately 251.08 g/mol. It typically presents as a white powder, with a melting point reported around 191°C. The presence of the bromine atom on the aromatic ring makes it highly amenable to cross-coupling reactions, such as Suzuki, Heck, or Sonogashira couplings, which are fundamental in constructing complex organic molecules. The carboxylic acid group offers another site for derivatization, including esterification, amidation, or reduction. These dual functionalities make it a powerful tool for chemists.
Regarding synthesis, 1-Bromo-2-naphthoic Acid can be prepared through several methods. A common laboratory approach involves the oxidation of a precursor like 1-bromo-2-hydroxymethyl naphthalene. This process typically uses oxidizing agents such as potassium permanganate under controlled conditions, followed by purification steps to achieve the desired high purity. Sourcing high-quality starting materials is critical for efficient synthesis. Researchers looking to buy 1-Bromo-2-naphthoic Acid can also find it readily available from specialized chemical manufacturers and suppliers, often offering it in various grades and quantities to suit research or production needs.
The demand for this compound is driven by its utility in both pharmaceutical intermediate synthesis and broader organic chemistry research. As a key building block, its reliable supply is crucial. When procuring from a manufacturer, inquiring about their production capabilities and quality assurance protocols is advisable. Understanding the typical synthesis routes employed by a supplier can also provide confidence in the product's consistency and purity. For those needing to buy 1-Bromo-2-naphthoic Acid, consulting with experienced chemical suppliers ensures access to a dependable source of this important organic chemistry reagent.
Perspectives & Insights
Core Pioneer 24
“Its unique structural features, including a brominated naphthalene ring coupled with a carboxylic acid functional group, dictate its chemical behavior and reactivity.”
Silicon Explorer X
“This article delves into the essential chemical properties of 1-Bromo-2-naphthoic Acid and discusses common synthesis routes, providing valuable insights for professionals looking to buy this compound.”
Quantum Catalyst AI
“The chemical identity of 1-Bromo-2-naphthoic Acid is defined by its molecular formula C11H7BrO2 and a molecular weight of approximately 251.”