Cas no 1564762-59-9 (2-methyl-5-(morpholin-4-yl)pentanoic acid)

2-Methyl-5-(morpholin-4-yl)pentanoic acid is a versatile intermediate in organic synthesis, particularly valued for its morpholine moiety, which enhances solubility and reactivity in various chemical transformations. Its structural features, including the carboxyl group and tertiary amine, make it useful in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. The compound exhibits favorable stability under standard conditions, facilitating handling and storage. Its compatibility with a range of reaction conditions allows for diverse functionalization, making it a valuable building block in medicinal chemistry and drug development. The morpholine ring further contributes to its potential as a precursor for bioactive molecules, particularly those targeting neurological and cardiovascular applications.
2-methyl-5-(morpholin-4-yl)pentanoic acid structure
1564762-59-9 structure
Product Name:2-methyl-5-(morpholin-4-yl)pentanoic acid
CAS No:1564762-59-9
MF:C10H19NO3
MW:201.262763261795
CID:6444930
PubChem ID:20751269
Update Time:2025-06-11

2-methyl-5-(morpholin-4-yl)pentanoic acid Chemical and Physical Properties

Names and Identifiers

    • 2-methyl-5-(morpholin-4-yl)pentanoic acid
    • EN300-1836902
    • 1564762-59-9
    • Inchi: 1S/C10H19NO3/c1-9(10(12)13)3-2-4-11-5-7-14-8-6-11/h9H,2-8H2,1H3,(H,12,13)
    • InChI Key: XIBUYKRVGPDPCD-UHFFFAOYSA-N
    • SMILES: O1CCN(CC1)CCCC(C(=O)O)C

Computed Properties

  • Exact Mass: 201.13649347g/mol
  • Monoisotopic Mass: 201.13649347g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 5
  • Complexity: 178
  • 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: -1.6
  • Topological Polar Surface Area: 49.8?2

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2-methyl-5-(morpholin-4-yl)pentanoic acid Related Literature

Additional information on 2-methyl-5-(morpholin-4-yl)pentanoic acid

Comprehensive Overview of 2-methyl-5-(morpholin-4-yl)pentanoic acid (CAS No. 1564762-59-9)

2-methyl-5-(morpholin-4-yl)pentanoic acid (CAS No. 1564762-59-9) is a specialized organic compound that has garnered significant attention in pharmaceutical and chemical research due to its unique structural features and potential applications. This compound, characterized by its morpholine and carboxylic acid functional groups, is often explored for its role in drug discovery, particularly in the development of small-molecule inhibitors and bioactive intermediates. Researchers are increasingly interested in its synthetic pathways, physicochemical properties, and biological activity, making it a subject of ongoing studies in medicinal chemistry.

The molecular structure of 2-methyl-5-(morpholin-4-yl)pentanoic acid includes a morpholine ring, which is known for enhancing solubility and bioavailability in drug candidates. This feature aligns with current trends in pharmaceutical development, where improving drug delivery systems and oral bioavailability are critical priorities. The compound's CAS No. 1564762-59-9 serves as a unique identifier in databases like PubChem and Reaxys, facilitating its study in high-throughput screening and structure-activity relationship (SAR) analyses. Its potential as a building block for more complex molecules further underscores its relevance in synthetic chemistry.

In recent years, the demand for custom synthesis and research chemicals like 2-methyl-5-(morpholin-4-yl)pentanoic acid has surged, driven by advancements in precision medicine and targeted therapy. This compound is frequently discussed in forums and publications focusing on kinase inhibitors and GPCR modulators, reflecting its versatility in drug design. Additionally, its stability under physiological conditions and compatibility with common coupling reagents make it a valuable tool for peptide and peptidomimetic synthesis.

From an industrial perspective, 2-methyl-5-(morpholin-4-yl)pentanoic acid is often procured by contract research organizations (CROs) and pharmaceutical companies for exploratory projects. Its scalable synthesis and cost-effective production are key factors driving its adoption. Furthermore, the compound's regulatory compliance and safety profile are frequently evaluated to ensure its suitability for large-scale applications. These aspects are particularly relevant given the growing emphasis on green chemistry and sustainable manufacturing practices.

In summary, 2-methyl-5-(morpholin-4-yl)pentanoic acid (CAS No. 1564762-59-9) represents a promising candidate for diverse applications in drug discovery and chemical synthesis. Its structural attributes, combined with its pharmacological potential, position it as a compound of interest for researchers and industry professionals alike. As the field of medicinal chemistry continues to evolve, this molecule is likely to play an increasingly important role in the development of next-generation therapeutics.

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