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Methyl 1-Phenylcyclopentane-1-carboxylate (CAS No. 4535-96-0): A Comprehensive Overview

Methyl 1-phenylcyclopentane-1-carboxylate (CAS No. 4535-96-0) is a versatile organic compound that has garnered significant attention in the fields of organic synthesis, pharmaceutical research, and materials science. This compound, characterized by its unique cyclopentane ring and phenyl substituent, offers a range of applications due to its structural properties and chemical reactivity.

The chemical structure of methyl 1-phenylcyclopentane-1-carboxylate consists of a cyclopentane ring with a carboxylic acid methyl ester group and a phenyl substituent attached to the same carbon atom. This configuration imparts specific physical and chemical properties that make it valuable in various scientific and industrial contexts. The compound is typically synthesized through the esterification of 1-phenylcyclopentanecarboxylic acid with methanol in the presence of an acid catalyst.

In recent years, methyl 1-phenylcyclopentane-1-carboxylate has been the subject of numerous studies aimed at exploring its potential in pharmaceutical development. One notable application is its use as an intermediate in the synthesis of bioactive molecules. For instance, researchers have utilized this compound as a building block in the synthesis of novel analgesics and anti-inflammatory agents. The cyclopentane ring and phenyl substituent provide a scaffold that can be further functionalized to introduce pharmacologically active groups.

Beyond pharmaceuticals, methyl 1-phenylcyclopentane-1-carboxylate has found applications in materials science. Its unique structure makes it suitable for use in the development of advanced polymers and coatings. The presence of the phenyl group enhances the compound's stability and mechanical properties, making it an attractive candidate for formulating high-performance materials. Recent studies have demonstrated its potential in creating thermally stable polymers with improved mechanical strength and durability.

The physical properties of methyl 1-phenylcyclopentane-1-carboxylate are also noteworthy. It is a colorless liquid at room temperature with a characteristic odor. The compound exhibits good solubility in organic solvents such as ethanol, acetone, and dichloromethane, which facilitates its use in various synthetic processes. Its boiling point is around 230°C at atmospheric pressure, making it suitable for distillation under reduced pressure conditions to avoid thermal decomposition.

In terms of safety and handling, methyl 1-phenylcyclopentane-1-carboxylate should be stored in a cool, dry place away from direct sunlight and incompatible materials. Proper personal protective equipment (PPE) should be used when handling this compound to minimize exposure risks. While it is not classified as a hazardous material under most regulatory frameworks, it is important to follow standard laboratory safety protocols to ensure safe handling and storage.

The environmental impact of methyl 1-phenylcyclopentane-1-carboxylate is another area of ongoing research. Studies have shown that this compound is biodegradable under aerobic conditions, reducing its potential for long-term environmental accumulation. However, responsible disposal practices are still recommended to minimize any adverse effects on ecosystems.

In conclusion, methyl 1-phenylcyclopentane-1-carboxylate (CAS No. 4535-96-0) is a multifaceted compound with significant potential in pharmaceutical research, materials science, and organic synthesis. Its unique structural features and chemical properties make it a valuable intermediate for developing novel bioactive molecules and advanced materials. As research continues to uncover new applications, this compound is likely to play an increasingly important role in various scientific and industrial fields.

• 36634-63-6(cyclopropanecarboxylic acid, 1,2-diphenyl-, methyl ester, trans-)
• 36634-64-7(cis-methyl 1,2-diphenylcyclopropane carboxylate)
• 933068-88-3(3-Cyclopentyl-2-phenylpropionic acid methyl ester)
• 66504-76-5(Dimethyl 1-(4-methylphenyl)-1,2-cyclopropanedicarboxylate)
• 4535-95-9(Cyclopentanecarboxylic acid, 1-phenyl-, ethyl ester)
• 17380-78-8(methyl 1-phenyl-1-cyclohexanecarboxylate)
• 1126651-95-3(Methyl 2,5,5-trimethyl-2-phenylhexanoate)
• 345618-40-8(1,2-Cyclopropanedicarboxylicacid, 1-(4-methylphenyl)-, 1,2-dimethyl ester)
• 62425-22-3(Octadecanoic acid, diphenyl-, methyl ester)
• 58469-03-7(Methyl 1-phenylcyclobutanecarboxylate)