Cas no 90646-25-6 (2-ethylcyclohexane-1-carboxylic acid)

2-ethylcyclohexane-1-carboxylic acid structure
90646-25-6 structure
Product Name:2-ethylcyclohexane-1-carboxylic acid
CAS No:90646-25-6
MF:C9H16O2
MW:156.222143173218
MDL:MFCD18901695
CID:3411115
PubChem ID:14048267
Update Time:2025-04-23

2-ethylcyclohexane-1-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • CYCLOHEXANECARBOXYLIC ACID, 2-ETHYL-
    • 2-ethylcyclohexane-1-carboxylic acid
    • EN300-194166
    • 2-ethylcyclohexane-1-carboxylicacid
    • 90646-25-6
    • SCHEMBL12942860
    • AKOS013175116
    • 971-783-2
    • Z1162465707
    • G49818
    • QDA64625
    • MDL: MFCD18901695
    • Inchi: 1S/C9H16O2/c1-2-7-5-3-4-6-8(7)9(10)11/h7-8H,2-6H2,1H3,(H,10,11)
    • InChI Key: BYSURPXRUHUJMH-UHFFFAOYSA-N
    • SMILES: OC(C1CCCCC1CC)=O

Computed Properties

  • Exact Mass: 156.115029749g/mol
  • Monoisotopic Mass: 156.115029749g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 143
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 2
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.8
  • Topological Polar Surface Area: 37.3?2

2-ethylcyclohexane-1-carboxylic acid Security Information

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Additional information on 2-ethylcyclohexane-1-carboxylic acid

CYCLOHEXANECARBOXYLIC ACID, 2-ETHYL- (CAS NO 90646-25-6): Applications and Research Developments in Modern Chemistry

Introducing CYCLOHEXANECARBOXYLIC ACID, 2-ETHYL-, a compound with the chemical identifier CAS NO 90646-25-6, which has garnered significant attention in the field of organic chemistry and pharmaceutical research. This compound, characterized by its unique molecular structure, presents a versatile platform for various chemical modifications and applications. The ethyl-substituted cyclohexanecarboxylic acid derivative is not only of academic interest but also holds promise for industrial applications, particularly in the synthesis of advanced materials and bioactive molecules.

The molecular structure of CYCLOHEXANECARBOXYLIC ACID, 2-ETHYL- consists of a cyclohexane ring substituted with a carboxylic acid group at the 1-position and an ethyl group at the 2-position. This configuration provides a stable backbone that can be further functionalized to suit specific chemical needs. The presence of both the carboxylic acid and ethyl groups makes this compound a valuable intermediate in organic synthesis, enabling the formation of esters, amides, and other derivatives that are crucial in pharmaceuticals and polymer chemistry.

In recent years, research on CYCLOHEXANECARBOXYLIC ACID, 2-ETHYL- has focused on its role as a building block in the synthesis of complex molecules. For instance, studies have demonstrated its utility in the preparation of novel heterocyclic compounds, which are known for their diverse biological activities. The ability to introduce various functional groups into the cyclohexane ring allows chemists to tailor the properties of these derivatives for specific applications, such as drug development and material science.

One of the most promising areas of research involving CYCLOHEXANECARBOXYLIC ACID, 2-ETHYL- is its application in pharmaceutical chemistry. Researchers have explored its potential as a precursor for nonsteroidal anti-inflammatory drugs (NSAIDs) and other therapeutic agents. The cyclohexane scaffold is commonly found in many biologically active molecules due to its ability to mimic natural products and facilitate interactions with biological targets. By modifying the substituents on this ring, scientists can fine-tune the pharmacological properties of the resulting compounds.

Moreover, the ethyl group in CYCLOHEXANECARBOXYLIC ACID, 2-ETHYL- contributes to its reactivity and flexibility in synthetic pathways. This feature has been exploited in the development of novel catalysts and ligands used in transition metal-catalyzed reactions. Such reactions are essential for constructing complex molecular architectures efficiently. The compound's compatibility with various reaction conditions makes it a preferred choice for researchers aiming to achieve high yields and selectivity in their synthetic endeavors.

The industrial relevance of CYCLOHEXANECARBOXYLIC ACID, 2-ETHYL- extends beyond pharmaceuticals to include polymer chemistry. Its derivatives can be incorporated into polymeric materials to enhance their mechanical properties or biodegradability. For example, researchers have investigated its use in creating biodegradable plastics by forming polyesters or polyamides derived from this compound. Such advancements align with global efforts to develop sustainable materials that minimize environmental impact.

In conclusion, CYCLOHEXANECARBOXYLIC ACID, 2-ETHYL- (CAS NO 90646-25-6) represents a fascinating subject of study with broad applications across multiple scientific disciplines. Its unique structural features make it an invaluable intermediate for synthesizing a wide range of bioactive molecules and advanced materials. As research continues to uncover new possibilities for this compound, its significance in modern chemistry is set to grow even further.

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