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Ethyl 2-(2-aminophenyl)acetate hydrochloride (CAS No. 61-88-1): A Comprehensive Overview

Ethyl 2-(2-aminophenyl)acetate hydrochloride (CAS No. 61-88-1) is a versatile compound with significant applications in the fields of pharmaceuticals, chemical synthesis, and biological research. This compound, also known as ethyl 2-(o-anilino)acetate hydrochloride, is a derivative of aniline and ethyl acetate, and it has gained attention due to its potential therapeutic properties and its role as an intermediate in the synthesis of various pharmaceuticals.

The molecular formula of Ethyl 2-(2-aminophenyl)acetate hydrochloride is C₁₀H₁₄ClNO₂, and its molecular weight is approximately 213.68 g/mol. The compound exists as a white crystalline solid with a melting point of around 150-153°C. Its solubility in water is moderate, and it is more soluble in organic solvents such as ethanol and methanol.

In the context of pharmaceutical research, Ethyl 2-(2-aminophenyl)acetate hydrochloride has been studied for its potential as a lead compound in the development of new drugs. Recent studies have highlighted its role in the synthesis of β-lactam antibiotics, which are crucial for treating bacterial infections. The compound's ability to form stable intermediates during chemical reactions makes it an attractive candidate for drug discovery and development.

Beyond its use in pharmaceuticals, Ethyl 2-(2-aminophenyl)acetate hydrochloride has also found applications in the field of chemical synthesis. It serves as a building block for the preparation of various organic compounds, including amines, esters, and amides. The versatility of this compound allows chemists to tailor its properties for specific applications, making it a valuable tool in synthetic chemistry.

In biological research, Ethyl 2-(2-aminophenyl)acetate hydrochloride has been investigated for its interactions with biological systems. Studies have shown that it can modulate the activity of certain enzymes and receptors, which may have implications for therapeutic applications. For instance, it has been found to inhibit the activity of cytochrome P450 enzymes, which are involved in drug metabolism and detoxification processes.

The safety profile of Ethyl 2-(2-aminophenyl)acetate hydrochloride is an important consideration in its use. While it is generally considered safe for laboratory use when proper handling procedures are followed, it is important to note that exposure to high concentrations may cause irritation to the eyes and skin. Therefore, appropriate personal protective equipment (PPE) should be used when handling this compound.

In terms of environmental impact, the disposal of Ethyl 2-(2-aminophenyl)acetate hydrochloride should be conducted in accordance with local regulations to prevent contamination of water sources and soil. Proper waste management practices are essential to ensure the safe disposal of this compound.

The market demand for Ethyl 2-(2-aminophenyl)acetate hydrochloride is driven by its diverse applications in pharmaceuticals, chemical synthesis, and research. As new studies continue to uncover its potential uses, the demand for this compound is expected to grow. Suppliers and manufacturers are increasingly focusing on improving production processes to meet the growing demand while maintaining high standards of quality and purity.

In conclusion, Ethyl 2-(2-aminophenyl)acetate hydrochloride (CAS No. 61-88-1) is a multifaceted compound with significant potential in various fields. Its role as a building block in chemical synthesis, its therapeutic properties, and its applications in biological research make it a valuable asset for researchers and industry professionals alike. As ongoing research continues to explore new avenues for its use, the future prospects for this compound appear promising.

• 49851-36-7(Methyl 2-(2-aminophenyl)acetate hydrochloride)
• 59235-35-7(Ethyl 2-(4-aminophenyl)acetate hydrochloride)
• 29640-92-4(Methyl 2-(2-amino-4-methylphenyl)acetate)
• 1341124-14-8(methyl 2-(2,6-diaminophenyl)acetate)
• 777062-28-9(Benzeneacetic acid, 2-amino-4-(1-hydroxyethyl)-, ethyl ester)
• 5438-70-0(Ethyl 4-Aminophenylacetate)
• 924309-78-4(Benzeneacetic acid, 4-amino-3-(1-methylethyl)-, ethyl ester)
• 35613-44-6(Methyl (2-amino-phenyl)-acetate)
• 400648-69-3(Benzeneacetic acid,3-amino-4-ethyl-, ethyl ester)
• 64460-85-1(ethyl 2-(2-aminophenyl)acetate)