Cas no 2060021-73-8 (1,2,4,4-Tetramethylcyclopentane-1-carboxylic acid)

1,2,4,4-Tetramethylcyclopentane-1-carboxylic acid is a substituted cyclopentane derivative featuring a carboxylic acid functional group and four methyl substituents. This compound is of interest in organic synthesis and pharmaceutical research due to its sterically hindered structure, which can influence reactivity and selectivity in chemical transformations. The presence of multiple methyl groups enhances its lipophilicity, making it potentially useful in the design of hydrophobic intermediates or active pharmaceutical ingredients (APIs). Its rigid cyclopentane backbone may also contribute to conformational stability in molecular applications. The carboxylic acid moiety allows for further functionalization, enabling its use as a building block in fine chemical synthesis.
1,2,4,4-Tetramethylcyclopentane-1-carboxylic acid structure
2060021-73-8 structure
Product Name:1,2,4,4-Tetramethylcyclopentane-1-carboxylic acid
CAS No:2060021-73-8
MF:C10H18O2
MW:170.248723506927
MDL:MFCD30487911
CID:5613622
PubChem ID:131550167
Update Time:2025-06-08

1,2,4,4-Tetramethylcyclopentane-1-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 1,2,4,4-Tetramethylcyclopentane-1-carboxylic acid
    • EN300-330197
    • 1,2,4,4-Tetramethylcyclopentane-1-carboxylicacid
    • 2060021-73-8
    • Cyclopentanecarboxylic acid, 1,2,4,4-tetramethyl-
    • MDL: MFCD30487911
    • Inchi: 1S/C10H18O2/c1-7-5-9(2,3)6-10(7,4)8(11)12/h7H,5-6H2,1-4H3,(H,11,12)
    • InChI Key: YUWQTBTVJFKYJA-UHFFFAOYSA-N
    • SMILES: OC(C1(C)CC(C)(C)CC1C)=O

Computed Properties

  • Exact Mass: 170.130679813g/mol
  • Monoisotopic Mass: 170.130679813g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 208
  • 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

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Additional information on 1,2,4,4-Tetramethylcyclopentane-1-carboxylic acid

Introduction to 1,2,4,4-Tetramethylcyclopentane-1-carboxylic Acid (CAS No. 2060021-73-8)

1,2,4,4-Tetramethylcyclopentane-1-carboxylic acid (CAS No. 2060021-73-8) is a unique and structurally complex 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 cyclopentane ring with four methyl groups and a carboxylic acid functional group, which imparts it with distinct chemical properties and reactivity.

The molecular structure of 1,2,4,4-tetramethylcyclopentane-1-carboxylic acid is of particular interest due to its high degree of symmetry and the presence of multiple methyl groups. These features contribute to its stability and make it an attractive candidate for use in the synthesis of more complex molecules. Recent studies have explored the synthetic routes to this compound, focusing on efficient and scalable methods that can be applied in both academic and industrial settings.

In the realm of pharmaceutical research, 1,2,4,4-tetramethylcyclopentane-1-carboxylic acid has shown promise as a building block for the development of novel drugs. Its unique structure allows for the introduction of various functional groups that can enhance the pharmacological properties of the final product. For instance, researchers have investigated its use in the synthesis of anti-inflammatory agents and antiviral compounds. The carboxylic acid group provides a reactive site for further functionalization, enabling the creation of derivatives with tailored biological activities.

Materials science is another area where 1,2,4,4-tetramethylcyclopentane-1-carboxylic acid has found applications. The compound's stability and reactivity make it suitable for use in the development of advanced materials such as polymers and coatings. Recent studies have demonstrated its potential in the synthesis of high-performance polymers with improved mechanical properties and thermal stability. These materials have potential applications in industries ranging from automotive to electronics.

The synthetic methods for producing 1,2,4,4-tetramethylcyclopentane-1-carboxylic acid have been extensively studied to optimize yield and purity. One notable approach involves the use of transition metal-catalyzed reactions, which offer high selectivity and efficiency. These methods are particularly valuable in large-scale production processes where cost-effectiveness and environmental sustainability are critical considerations.

In addition to its synthetic utility, 1,2,4,4-tetramethylcyclopentane-1-carboxylic acid has been investigated for its potential as a chiral building block in asymmetric synthesis. The presence of multiple chiral centers within the molecule makes it an ideal candidate for creating enantiomerically pure compounds. This property is crucial in pharmaceuticals where enantiomeric purity can significantly impact drug efficacy and safety.

The physical properties of 1,2,4,4-tetramethylcyclopentane-1-carboxylic acid, such as its melting point and solubility characteristics, have also been studied in detail. These properties are essential for optimizing its use in various applications. For example, understanding its solubility behavior can aid in developing effective formulations for drug delivery systems.

To further enhance its utility in research and development, ongoing efforts are focused on developing new derivatives of 1,2,4,4-tetramethylcyclopentane-1-carboxylic acid. These derivatives are designed to possess specific functional groups that can confer additional properties or functionalities to the molecule. For instance, esterification reactions can produce ester derivatives with improved solubility or biodegradability.

In conclusion, 1,2,4,4-tetramethylcyclopentane-1-carboxylic acid (CAS No. 2060021-73-8) is a versatile compound with a wide range of potential applications in pharmaceuticals, materials science, and chemical synthesis. Its unique molecular structure and reactivity make it an attractive candidate for further research and development. As new synthetic methods and applications continue to emerge, this compound is likely to play an increasingly important role in advancing scientific knowledge and technological innovation.

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