Cas no 91536-65-1 ((prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine)

Technical Introduction: (Prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine is a bifunctional amine compound featuring both allyloxy and propargyl groups, making it a versatile intermediate in organic synthesis. Its dual reactivity allows for selective modifications via click chemistry (alkyne-azide cycloaddition) or thiol-ene reactions, facilitating applications in polymer chemistry, bioconjugation, and pharmaceutical derivatization. The compound’s structure enables efficient crosslinking or functionalization under mild conditions, enhancing its utility in materials science and medicinal chemistry. High purity grades ensure reproducibility in research and industrial processes. Stability under standard conditions and compatibility with a range of solvents further contribute to its broad applicability.
(prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine structure
91536-65-1 structure
Product Name:(prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine
CAS No:91536-65-1
MF:C6H9NO
MW:111.141761541367
CID:4311953
Update Time:2025-06-14

(prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine Chemical and Physical Properties

Names and Identifiers

    • 2-Propyn-1-amine, N-(2-propenyloxy)-
    • 2-Propyn-1-amine, N-(2-propen-1-yloxy)-
    • (prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine
    • Inchi: 1S/C6H9NO/c1-3-5-7-8-6-4-2/h1,4,7H,2,5-6H2
    • InChI Key: IKDGNMPBZXJVKM-UHFFFAOYSA-N
    • SMILES: C(NOCC=C)C#C

(prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine Pricemore >>

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(prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine Related Literature

Additional information on (prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine

Comprehensive Overview of (prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine (CAS No. 91536-65-1)

The chemical compound (prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine (CAS No. 91536-65-1) is a specialized organic molecule that has garnered significant attention in recent years due to its unique structural properties and potential applications in various fields. This compound, characterized by its allyloxy and propargylamine functional groups, is often explored in the context of click chemistry, polymer science, and pharmaceutical intermediates. Its dual reactivity, stemming from the presence of both alkene and alkyne moieties, makes it a versatile building block for synthetic chemists.

In the realm of green chemistry, researchers are increasingly focusing on sustainable synthesis methods for compounds like (prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine. The demand for eco-friendly solvents and catalyst-free reactions has led to innovative approaches in its production. For instance, recent studies highlight the use of biodegradable catalysts to minimize environmental impact while maintaining high yields. This aligns with the growing consumer and industrial interest in sustainable chemicals and circular economy principles.

Another area where (prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine shows promise is in the development of advanced materials. Its ability to participate in cross-linking reactions makes it a valuable component in the creation of self-healing polymers and smart coatings. These materials are particularly relevant in industries such as automotive, aerospace, and electronics, where durability and performance are critical. The compound’s thermosetting properties further enhance its utility in high-temperature applications.

From a pharmaceutical perspective, (prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine serves as a key intermediate in the synthesis of bioactive molecules. Its propargylamine moiety is often incorporated into drug candidates targeting neurodegenerative diseases, such as Alzheimer’s and Parkinson’s. This has sparked interest among researchers exploring neuroprotective agents and enzyme inhibitors. The compound’s modularity allows for rapid diversification, a feature highly valued in drug discovery pipelines.

In the context of industrial applications, (prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine is utilized in the formulation of adhesives and sealants. Its dual-functional reactivity enables strong bonding with various substrates, making it ideal for high-performance composites. Additionally, the compound’s compatibility with UV-curing technologies has expanded its use in 3D printing resins and photopolymerization processes. These applications are particularly relevant in the era of additive manufacturing and customized production.

The safety profile of (prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine is another topic of interest. While it is not classified as a hazardous substance, proper handling protocols are recommended to ensure workplace safety. Recent advancements in predictive toxicology and computational modeling have provided deeper insights into its biodegradability and ecotoxicological effects. These tools are increasingly used to assess the environmental impact of chemical compounds, addressing concerns raised by regulatory agencies and stakeholders.

Looking ahead, the future of (prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine lies in its integration with emerging technologies. For example, its potential role in nanomaterial synthesis and molecular electronics is being explored. The compound’s ability to form conjugated systems could pave the way for innovations in organic semiconductors and optoelectronic devices. As the demand for renewable energy solutions grows, such applications could become increasingly significant.

In summary, (prop-2-en-1-yloxy)(prop-2-yn-1-yl)amine (CAS No. 91536-65-1) is a multifaceted compound with wide-ranging applications. Its relevance in sustainable chemistry, material science, and pharmaceutical research underscores its importance in modern scientific and industrial landscapes. By leveraging its unique properties, researchers and manufacturers can continue to unlock new possibilities in innovation and technology.

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