Cas no 1575-73-1 (2-ethylpent-4-enoic acid)

2-Ethylpent-4-enoic acid is an unsaturated carboxylic acid characterized by its five-carbon backbone with an ethyl substituent at the second position and a double bond at the fourth carbon. This structure imparts reactivity suitable for applications in organic synthesis, particularly in the production of specialty polymers, fine chemicals, and intermediates. The presence of both a carboxylic acid group and an alkene functionality allows for versatile derivatization, including esterification, amidation, or addition reactions. Its moderate acidity and compatibility with various reaction conditions make it a useful building block in pharmaceutical and agrochemical research. The compound is typically handled under inert conditions to preserve its unsaturated moiety.
2-ethylpent-4-enoic acid structure
2-ethylpent-4-enoic acid structure
Product Name:2-ethylpent-4-enoic acid
CAS No:1575-73-1
MF:C7H12O2
MW:128.168982505798
MDL:MFCD19228159
CID:230911
PubChem ID:297238
Update Time:2025-06-26

2-ethylpent-4-enoic acid Chemical and Physical Properties

Names and Identifiers

    • 4-Pentenoic acid,2-ethyl-
    • 2-ethylpent-4-enoic acid
    • 2-Aethyl-pent-4-ensaeure
    • 2-allylbutyric acid
    • 2-ethyl-4-pentenoic acid
    • 2-ethyl-pent-4-enoic acid
    • 4-Pentenoic acid, 2-ethyl
    • AC1L6RC0
    • AGN-PC-0052HU
    • allylethylacetic acid
    • NSC168189
    • BAA57573
    • DTXSID40304913
    • 2-ETHYLPENT-4-ENOICACID
    • ethyl 4-pentenoic acid
    • SCHEMBL629461
    • NSC-168189
    • CS-0240003
    • 1575-73-1
    • F95366
    • EN300-222611
    • NSC 168189
    • AKOS006375838
    • MDL: MFCD19228159
    • Inchi: 1S/C7H12O2/c1-3-5-6(4-2)7(8)9/h3,6H,1,4-5H2,2H3,(H,8,9)
    • InChI Key: MCEBMFWJKMJTPD-UHFFFAOYSA-N
    • SMILES: OC(C(CC=C)CC)=O

Computed Properties

  • Exact Mass: 128.08376
  • Monoisotopic Mass: 128.084
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 4
  • Complexity: 108
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.8
  • Topological Polar Surface Area: 37.3?2

Experimental Properties

  • Density: 0.955
  • Boiling Point: 209.9°Cat760mmHg
  • Flash Point: 107.3°C
  • Refractive Index: 1.445
  • PSA: 37.3
  • LogP: 1.67330

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Additional information on 2-ethylpent-4-enoic acid

Professional Introduction to 2-ethylpent-4-enoic acid (CAS No. 1575-73-1)

2-ethylpent-4-enoic acid, with the chemical formula C7H12O2, is a significant compound in the field of organic chemistry and pharmaceutical research. Its CAS number, 1575-73-1, uniquely identifies it in scientific literature and industrial applications. This compound, classified as an unsaturated carboxylic acid derivative, has garnered attention due to its versatile chemical properties and potential applications in drug synthesis and biochemical pathways.

The molecular structure of 2-ethylpent-4-enoic acid features a pentyl chain with an ethyl substituent at the second carbon and a double bond between the fourth and fifth carbons. This configuration contributes to its reactivity, making it a valuable intermediate in organic synthesis. The presence of both a carboxylic acid group and an alkene double bond allows for diverse functionalization, enabling the development of complex molecules with tailored biological activities.

In recent years, research on 2-ethylpent-4-enoic acid has expanded significantly, particularly in the context of medicinal chemistry. Studies have demonstrated its role as a precursor in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs) and other pharmacologically active compounds. The compound’s ability to undergo various chemical transformations, such as esterification, hydrogenation, and oxidation, makes it a cornerstone in the development of novel therapeutic agents.

One of the most compelling aspects of 2-ethylpent-4-enoic acid is its potential in modulating metabolic pathways. Emerging research suggests that derivatives of this compound may influence lipid metabolism and have anti-inflammatory effects. For instance, studies have explored its interaction with enzymes involved in fatty acid biosynthesis, indicating possible applications in managing metabolic disorders such as obesity and type 2 diabetes. These findings highlight the compound’s significance in addressing contemporary healthcare challenges.

The pharmaceutical industry has also shown interest in 2-ethylpent-4-enoic acid due to its structural similarity to naturally occurring fatty acids. This resemblance facilitates its incorporation into drug formulations, enhancing bioavailability and reducing toxicity. Furthermore, its role as a chiral building block allows for the synthesis of enantiomerically pure compounds, which are often crucial for achieving optimal pharmacological outcomes. Such attributes position 2-ethylpent-4-enoic acid as a key player in the next generation of drug development.

Advances in synthetic methodologies have further propelled the utility of 2-ethylpent-4-enoic acid. Modern techniques, including catalytic asymmetric hydrogenation and flow chemistry, enable more efficient and scalable production processes. These innovations not only reduce costs but also improve the sustainability of manufacturing operations. As a result, researchers can now explore more complex derivatives with greater ease, accelerating the discovery of new therapeutic entities.

The biochemical properties of 2-ethylpent-4-enoic acid also make it relevant in agricultural science. Researchers are investigating its potential as a plant growth regulator or pesticide precursor due to its ability to interact with biological systems at low concentrations. Such applications could contribute to developing environmentally friendly solutions for crop protection and yield enhancement.

In conclusion, 2-ethylpent-4-enoic acid (CAS No. 1575-73-1) is a multifaceted compound with broad applications across chemistry and medicine. Its unique structural features and reactivity make it indispensable in drug synthesis and metabolic research. As scientific understanding evolves, new opportunities for leveraging this compound are likely to emerge, reinforcing its importance in both academic and industrial settings.

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