8-(2-Hydroxy-benzolylamino)octanoic acid ethylester
[CAS# 1027911-46-1]

Identification

• Classification: Organic raw materials >> Carboxylic compounds and derivatives >> Carboxylic esters and their derivatives
• Name: 8-(2-Hydroxy-benzolylamino)octanoic acid ethylester
• Synonyms: ethyl 8-(2-hydroxyanilino)octanoate
• Molecular Formula: C₁₆H₂₅NO₃
• Molecular Weight: 279.37
• CAS Registry Number: 1027911-46-1
• SMILES: CCOC(=O)CCCCCCCNC1=CC=CC=C1O

Discovory and Applicatios

8-(2-Hydroxy-benzoylamino)octanoic acid ethyl ester is a synthetic compound of interest in the pharmaceutical and materials sciences due to its unique structural properties and potential applications. This molecule features a combination of hydrophobic and hydrophilic functional groups, making it suitable for diverse roles in molecular design and biological activity studies.

The compound’s synthesis involves the condensation of 2-hydroxybenzoic acid derivatives with octanoic acid precursors, followed by esterification. This process allows precise tailoring of the molecule's structure for desired chemical reactivity and physical properties. Its development builds on foundational work in amide chemistry, which has long been utilized to design bioactive compounds and materials with tailored interactions.

One of the primary areas of interest for 8-(2-hydroxy-benzoylamino)octanoic acid ethyl ester is its potential as a bioactive molecule. The presence of the 2-hydroxybenzoyl group, a motif often associated with biological activity, has led researchers to explore its properties as a ligand for metal ions or enzymes. Such studies aim to assess its efficacy in pharmaceutical applications, including as a precursor for drugs targeting metabolic or oxidative pathways.

In materials science, the compound's amphiphilic structure enables its use in the design of functional coatings or delivery systems. For instance, the ethyl ester moiety offers solubility in organic solvents, facilitating its incorporation into polymers or surface treatments. Its hydrophilic benzoyl functionality and hydrophobic alkyl chain make it a candidate for self-assembling systems in emulsifiers, stabilizers, or nanomaterials.

Another potential application lies in analytical chemistry, where derivatives of this compound may be used as probes or reagents. The 2-hydroxy group can participate in hydrogen bonding and coordination chemistry, providing a versatile platform for interaction studies in complex chemical systems.

The compound has also garnered attention for its potential in agricultural and cosmetic formulations. Its structural features suggest compatibility with formulations requiring amphiphilic additives, such as emulsifiers or stabilizing agents, and its benzoylamino group may confer additional functional benefits, such as UV absorption or antioxidative properties.

Current research efforts are focused on expanding the understanding of 8-(2-hydroxy-benzoylamino)octanoic acid ethyl ester’s chemical behavior and optimizing its synthesis for large-scale production. Furthermore, its potential environmental impact and biocompatibility are being studied to ensure its safety for diverse applications.