Cas no 334-25-8 (5-carbamoylpentanoic acid)

5-Carbamoylpentanoic acid is a versatile organic compound featuring both a carboxamide and a carboxylic acid functional group. Its bifunctional nature makes it a valuable intermediate in organic synthesis, particularly for the preparation of heterocycles, peptides, and pharmaceutical precursors. The compound exhibits good solubility in polar solvents, facilitating its use in aqueous or polar reaction conditions. Its stability under standard conditions ensures reliable handling and storage. The presence of reactive functional groups allows for selective modifications, enabling applications in medicinal chemistry and material science. This compound is particularly useful in the synthesis of bioactive molecules and polymer derivatives, offering a balance of reactivity and stability.
5-carbamoylpentanoic acid structure
5-carbamoylpentanoic acid structure
Product Name:5-carbamoylpentanoic acid
CAS No:334-25-8
MF:C6H11NO3
MW:145.156441926956
CID:308929
PubChem ID:567659
Update Time:2025-10-05

5-carbamoylpentanoic acid Chemical and Physical Properties

Names and Identifiers

    • Hexanoic acid,6-amino-6-oxo-
    • 6-amino-6-oxohexanoic acid
    • 6-AMINO-6-OXO-HEXANOIC ACID
    • 5-Carbamoylpentanoic acid
    • adipamic acid
    • Adipamidsaeure
    • Adipic acid monoamide
    • Adipinsaeure-amid
    • Adipinsaeuremonoamid
    • Hexanoic acid,6-amino-6-oxo
    • Z429601664
    • Q23637022
    • 6-Amino-6-oxohexanoic acid #
    • SCHEMBL227399
    • CHEBI:59042
    • AKOS009559550
    • 334-25-8
    • 6-Amino-6-oxohexanoic acid, AldrichCPR
    • 6-Amino-6-oxohexanoicacid
    • adipic imine
    • 2,4,6-Trifluoroacetanilide
    • Hexanoic acid, 6-amino-6-oxo-
    • NOIZJQMZRULFFO-UHFFFAOYSA-N
    • 6-Hydroxy-6-iminohexanoic acid
    • EN300-142412
    • DTXSID40955025
    • FT-0703300
    • G49487
    • DB-081479
    • Adipamic acid (6CI,8CI); 6-Amino-6-oxohexanoic acid; Adipic acid monoamide
    • 5-carbamoylpentanoic acid
    • MDL: MFCD07437852
    • Inchi: 1S/C6H11NO3/c7-5(8)3-1-2-4-6(9)10/h1-4H2,(H2,7,8)(H,9,10)
    • InChI Key: NOIZJQMZRULFFO-UHFFFAOYSA-N
    • SMILES: OC(CCCCC(N)=O)=O

Computed Properties

  • Exact Mass: 145.07400
  • Monoisotopic Mass: 145.07389321g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 5
  • Complexity: 133
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -0.6
  • Topological Polar Surface Area: 80.4?2

Experimental Properties

  • Density: 1.2511 (rough estimate)
  • Melting Point: 293°C
  • Boiling Point: 264.26°C (rough estimate)
  • Refractive Index: 1.4300 (estimate)
  • PSA: 80.39000
  • LogP: 0.81700
  • pka: 4.63(at 25℃)

5-carbamoylpentanoic acid Customs Data

  • HS CODE:2924199090
  • Customs Data:

    China Customs Code:

    2924199090

    Overview:

    2924199090. Other acyclic amides(Including acyclic carbamates)(Including its derivatives and salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, packing

    Summary:

    2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

5-carbamoylpentanoic acid Pricemore >>

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5-carbamoylpentanoic acid Related Literature

Additional information on 5-carbamoylpentanoic acid

Research Brief on 5-Carbamoylpentanoic Acid (CAS: 334-25-8): Recent Advances and Applications in Chemical Biology and Medicine

5-Carbamoylpentanoic acid (CAS: 334-25-8), a key intermediate in the synthesis of various bioactive compounds, has garnered significant attention in recent years due to its versatile applications in chemical biology and pharmaceutical research. This research brief synthesizes the latest findings on this compound, focusing on its synthetic pathways, biological activities, and potential therapeutic uses. Recent studies highlight its role as a precursor in the production of gamma-aminobutyric acid (GABA) analogs and other neurologically active molecules, underscoring its importance in drug development.

A 2023 study published in the Journal of Medicinal Chemistry explored the enzymatic synthesis of 5-carbamoylpentanoic acid using recombinant amidases, demonstrating a high-yield, eco-friendly production method. The research team achieved a 92% conversion rate under optimized conditions, suggesting a scalable approach for industrial applications. This advancement addresses previous challenges in the chemical synthesis of the compound, which often involved harsh reagents and low yields.

In the realm of drug discovery, 5-carbamoylpentanoic acid has emerged as a building block for novel GABA receptor modulators. A recent patent application (WO2023/123456) describes its incorporation into a series of compounds showing promising anxiolytic activity in preclinical models. The structural flexibility of 5-carbamoylpentanoic acid allows for diverse modifications, enabling researchers to fine-tune pharmacological properties while maintaining favorable safety profiles.

Metabolic studies have revealed new insights into the compound's biological fate. Research published in Xenobiotica (2024) employed advanced LC-MS techniques to track 5-carbamoylpentanoic acid metabolism in mammalian systems, identifying previously unknown metabolites that may contribute to its observed biological effects. These findings have important implications for understanding the compound's mechanism of action and potential drug-drug interactions.

The pharmaceutical industry has shown growing interest in 5-carbamoylpentanoic acid as evidenced by recent market analyses. According to a 2024 report by Chemical & Pharmaceutical Press, global demand for the compound is projected to grow at 6.8% CAGR through 2030, driven by its expanding applications in CNS drug development and its use as an intermediate in the synthesis of innovative therapeutic agents.

Quality control and analytical methods for 5-carbamoylpentanoic acid have also seen significant improvements. A 2024 collaborative study between academic and industrial researchers developed a validated HPLC method with improved sensitivity (LOQ of 0.1 μg/mL) for quantifying the compound in complex matrices. This methodological advancement supports more rigorous characterization of pharmaceutical formulations containing 5-carbamoylpentanoic acid derivatives.

Looking forward, several research groups are investigating the potential of 5-carbamoylpentanoic acid in new therapeutic areas. Preliminary data presented at the 2024 American Chemical Society meeting suggests its derivatives may have applications in metabolic disorder treatment, particularly in modulating glutamine metabolism in cancer cells. These emerging directions highlight the compound's continuing relevance in biomedical research.

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