Cas no 1306615-57-5 (pent-3-en-1-amine hydrochloride)

Pent-3-en-1-amine hydrochloride is a versatile organic compound featuring an amine group and an unsaturated pentene chain, rendered stable and soluble in its hydrochloride salt form. This intermediate is particularly valuable in synthetic organic chemistry, serving as a building block for pharmaceuticals, agrochemicals, and specialty materials. Its reactive double bond allows for further functionalization, while the hydrochloride form enhances handling and storage stability. The compound is characterized by high purity and consistent performance, making it suitable for precision applications in research and industrial synthesis. Its structural properties enable efficient incorporation into complex molecular frameworks, supporting diverse chemical transformations.
pent-3-en-1-amine hydrochloride structure
1306615-57-5 structure
Product Name:pent-3-en-1-amine hydrochloride
CAS No:1306615-57-5
MF:C5H12ClN
MW:121.608480453491
CID:4587282
Update Time:2025-10-29

pent-3-en-1-amine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 3-Penten-1-amine, hydrochloride (1:1)
    • pent-3-en-1-amine hydrochloride
    • Inchi: 1S/C5H11N.ClH/c1-2-3-4-5-6;/h2-3H,4-6H2,1H3;1H
    • InChI Key: JKIHNQMXIWMLLE-UHFFFAOYSA-N
    • SMILES: C(=CC)CCN.Cl

pent-3-en-1-amine hydrochloride Security Information

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$ 70.00 2022-06-07
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$ 95.00 2022-06-07
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Additional information on pent-3-en-1-amine hydrochloride

Pent-3-en-1-amine Hydrochloride (CAS No. 1306615-57-5): An Overview and Recent Advances

Pent-3-en-1-amine hydrochloride (CAS No. 1306615-57-5) is a versatile organic compound that has garnered significant attention in the fields of medicinal chemistry and pharmaceutical research. This compound, also known as allylamine hydrochloride, is characterized by its unique chemical structure, which includes a double bond at the third carbon position of the pentane chain and an amine group at the first carbon position. The hydrochloride salt form enhances its solubility and stability, making it a valuable intermediate in various synthetic pathways.

The chemical formula of pent-3-en-1-amine hydrochloride is C5H12N·HCl, with a molecular weight of approximately 129.62 g/mol. Its physical properties include a melting point of around 48°C and a boiling point of approximately 170°C. The compound is highly soluble in water and polar organic solvents, which facilitates its use in a wide range of chemical reactions and processes.

In recent years, pent-3-en-1-amine hydrochloride has been extensively studied for its potential applications in the development of novel pharmaceuticals. One of the key areas of interest is its role as a building block in the synthesis of bioactive compounds. For instance, researchers have explored its use in the synthesis of antiviral agents, particularly those targeting viral proteases. A study published in the Journal of Medicinal Chemistry highlighted the effectiveness of derivatives of pent-3-en-1-amine hydrochloride in inhibiting the activity of viral proteases, suggesting potential therapeutic applications in the treatment of viral infections.

Beyond antiviral research, pent-3-en-1-amine hydrochloride has also shown promise in the development of anti-inflammatory drugs. Inflammation is a complex biological response involving various mediators and signaling pathways. A recent study in the European Journal of Medicinal Chemistry demonstrated that derivatives of pent-3-en-1-amine hydrochloride exhibit potent anti-inflammatory activity by modulating key inflammatory cytokines such as TNF-alpha and IL-6. These findings suggest that this compound could be a valuable starting point for the design of new anti-inflammatory agents.

The synthetic versatility of pent-3-en-1-amine hydrochloride has also been leveraged in the development of prodrugs. Prodrugs are biologically inactive compounds that are converted into their active forms through metabolic processes within the body. A study published in Organic & Biomolecular Chemistry reported the successful synthesis of prodrugs derived from pent-3-en-1-amine hydrochloride, which showed improved pharmacokinetic properties and enhanced therapeutic efficacy compared to their parent compounds. This research highlights the potential of this compound as a platform for developing more effective and targeted therapies.

In addition to its pharmaceutical applications, pent-3-en-1-amine hydrochloride has found use in other areas such as materials science and analytical chemistry. For example, it has been employed as a ligand in coordination chemistry to form stable complexes with various metal ions. These complexes have shown interesting properties, such as luminescence and catalytic activity, which could be exploited for developing new materials with unique functionalities.

The environmental impact and safety profile of pent-3-en-1-amine hydrochloride are also important considerations for its industrial use. Studies have shown that this compound is relatively stable under standard laboratory conditions but can decompose at high temperatures or in strongly acidic or basic environments. Proper handling and storage practices are essential to ensure its stability and prevent any potential hazards.

In conclusion, pent-3-en-1-amine hydrochloride (CAS No. 1306615-57-5) is a multifaceted compound with significant potential in various scientific and industrial applications. Its unique chemical structure and synthetic versatility make it an attractive candidate for further research and development, particularly in the fields of medicinal chemistry and pharmaceuticals. As ongoing studies continue to uncover new properties and applications, this compound is likely to play an increasingly important role in advancing our understanding and capabilities in these areas.

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