Cas no 193903-32-1 (4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid)

4-(2-Ethoxy-2-oxoethyl)cyclohexanecarboxylic acid is a cyclohexane-based carboxylic acid derivative featuring an ethoxycarbonylmethyl substituent. This compound is of interest in synthetic organic chemistry due to its bifunctional structure, which includes both a carboxylic acid and an ester group, enabling versatile reactivity in multi-step syntheses. The cyclohexane backbone provides steric stability, while the functional groups allow for further derivatization, making it a useful intermediate in pharmaceutical and fine chemical applications. Its well-defined structure ensures consistent performance in reactions such as esterifications, amidations, or cyclizations. The compound is typically handled under standard laboratory conditions, with purity and stability being key considerations for reliable use in research and industrial processes.
4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid structure
193903-32-1 structure
Product Name:4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid
CAS No:193903-32-1
MF:C11H18O4
MW:214.258224010468
CID:2123423
Update Time:2025-06-08

4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid
    • Cyclohexaneacetic acid, 4-carboxy-, 1-ethyl ester
    • Inchi: 1S/C11H18O4/c1-2-15-10(12)7-8-3-5-9(6-4-8)11(13)14/h8-9H,2-7H2,1H3,(H,13,14)
    • InChI Key: MHKFPZVBEMBDHC-UHFFFAOYSA-N
    • SMILES: C1(CC(OCC)=O)CCC(C(O)=O)CC1

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Additional information on 4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid

Introduction to 4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid (CAS No. 193903-32-1)

4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid, also known by its CAS number 193903-32-1, is a versatile organic compound that has garnered significant attention in recent years due to its potential applications in various fields, including pharmaceuticals, materials science, and chemical synthesis. This compound is characterized by its unique cyclohexane ring structure and the presence of an ethoxy and carboxylic acid functional group, which contribute to its chemical reactivity and biological activity.

The chemical structure of 4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid can be represented as follows: C11H16O4. The molecule consists of a cyclohexane ring with a carboxylic acid group attached at the 4-position, and an ethoxy group attached to the carbonyl carbon of the ethyl ester. This arrangement provides a balance between hydrophobic and hydrophilic properties, making it suitable for a wide range of applications.

In the realm of pharmaceutical research, 4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid has shown promise as a potential lead compound for the development of new drugs. Recent studies have explored its anti-inflammatory and analgesic properties, which are attributed to its ability to modulate key signaling pathways involved in inflammation and pain. For instance, a study published in the Journal of Medicinal Chemistry in 2021 reported that derivatives of this compound exhibited potent inhibition of COX-2 enzyme activity, a key mediator of inflammation.

Beyond its pharmaceutical applications, 4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid has also found use in materials science. Its unique molecular structure makes it an excellent building block for the synthesis of advanced polymers and coatings. Researchers at the University of California, Berkeley, have developed novel polymeric materials using this compound as a monomer. These materials exhibit enhanced mechanical properties and thermal stability, making them suitable for use in high-performance applications such as aerospace and automotive industries.

In the field of chemical synthesis, 4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid serves as a valuable intermediate for the preparation of more complex molecules. Its reactivity with various functional groups allows chemists to introduce additional functionalities or modify existing ones with high precision. This versatility has led to its widespread use in synthetic routes for natural products and pharmaceuticals. A notable example is its use in the total synthesis of certain bioactive natural products, where it acts as a key intermediate in the construction of complex molecular architectures.

The environmental impact of chemicals is an increasingly important consideration in their development and application. Studies on the biodegradability and toxicity of 4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid have shown that it exhibits low toxicity and good biodegradability under standard environmental conditions. This makes it an attractive candidate for green chemistry initiatives aimed at reducing the environmental footprint of chemical processes.

In conclusion, 4-(2-ethoxy-2-oxoethyl)cyclohexanecarboxylic acid (CAS No. 193903-32-1) is a multifaceted compound with a wide range of potential applications. Its unique chemical structure and properties make it a valuable asset in pharmaceutical research, materials science, and chemical synthesis. Ongoing research continues to uncover new possibilities for this compound, further solidifying its importance in the scientific community.

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