Cas no 57536-91-1 (1-(naphthalen-2-yl)piperazine)

1-(naphthalen-2-yl)piperazine structure
1-(naphthalen-2-yl)piperazine structure
Product Name:1-(naphthalen-2-yl)piperazine
CAS No:57536-91-1
MF:C14H16N2
MW:212.290243148804
CID:844862
Update Time:2026-04-29

1-(naphthalen-2-yl)piperazine Chemical and Physical Properties

Names and Identifiers

    • 1-(2-NAPHTHYL)PIPERAZINE
    • 1-(2-Naphthyl)piperazine dihydrochloride
    • 1-(naphthalen-2-yl)piperazine
    • 1-NAPHTHALEN-2-YL-PIPERAZINE DIHYDROCHLORIDE
    • 1-b-Naphthylpiperazine
    • 3-naphthyl piperazine

Computed Properties

  • Exact Mass: 212.13100

Experimental Properties

  • PSA: 15.27000
  • LogP: 2.64320

1-(naphthalen-2-yl)piperazine Customs Data

  • HS CODE:2933599090
  • Customs Data:

    China Customs Code:

    2933599090

    Overview:

    2933599090. Other compounds with pyrimidine ring in structure(Including other compounds with piperazine ring on the structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

1-(naphthalen-2-yl)piperazine Pricemore >>

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Additional information on 1-(naphthalen-2-yl)piperazine

1-(Naphthalen-2-yl)piperazine: A Versatile Chemical Compound with Diverse Applications

1-(Naphthalen-2-yl)piperazine (CAS No. 57536-91-1) is a specialized organic compound that has garnered significant attention in both academic and industrial research. This compound, which combines a naphthalene ring with a piperazine moiety, exhibits unique chemical properties that make it valuable in various applications, including pharmaceuticals, material science, and chemical synthesis. Its molecular structure, characterized by the fusion of aromatic and heterocyclic components, allows for versatile reactivity and functionalization, making it a key intermediate in numerous synthetic pathways.

The growing interest in 1-(naphthalen-2-yl)piperazine derivatives is driven by their potential in drug discovery and development. Researchers are particularly intrigued by its role as a building block for central nervous system (CNS) targeting molecules, given the piperazine group's prevalence in bioactive compounds. Recent studies have explored its utility in designing ligands for neurotransmitter receptors, which aligns with the increasing demand for novel neuropharmacological agents. This trend is reflected in the rising number of searches for "piperazine-based drug design" and "naphthalene derivatives in medicine" across scientific databases and AI-driven research tools.

From a chemical perspective, 1-(naphthalen-2-yl)piperazine demonstrates notable stability and solubility characteristics. Its aromatic naphthalene core contributes to enhanced lipophilicity, while the piperazine nitrogen atoms offer sites for hydrogen bonding and protonation. These features make it an attractive candidate for applications in organic electronics and fluorescence-based sensors, areas that have seen exponential growth due to advancements in nanotechnology and diagnostic tools. Industry professionals frequently search for terms like "naphthalene piperazine synthesis" and "applications of heterocyclic naphthalenes," highlighting the compound's relevance in cutting-edge research.

The synthesis of 1-(naphthalen-2-yl)piperazine typically involves the coupling of 2-bromonaphthalene with piperazine under palladium-catalyzed conditions, a method that has been optimized for high yield and purity. Recent innovations in green chemistry have also introduced more sustainable approaches, such as microwave-assisted reactions, which reduce energy consumption and reaction times. These developments resonate with the global push toward environmentally friendly chemical processes, a topic frequently queried in academic and industrial forums.

In material science, 1-(naphthalen-2-yl)piperazine has shown promise as a precursor for conducting polymers and luminescent materials. Its ability to form stable complexes with metals and other organic molecules has opened doors for applications in optoelectronic devices and catalysis. Searches for "naphthalene-based functional materials" and "piperazine in polymer chemistry" underscore the compound's interdisciplinary appeal.

Quality control and analytical characterization of 1-(naphthalen-2-yl)piperazine are critical for ensuring its performance in various applications. Techniques such as high-performance liquid chromatography (HPLC), nuclear magnetic resonance (NMR) spectroscopy, and mass spectrometry are commonly employed to verify purity and structural integrity. These methods align with the increasing emphasis on quality assurance in chemical manufacturing, a concern frequently raised in industry-specific searches.

The commercial availability of 1-(naphthalen-2-yl)piperazine has expanded in recent years, with suppliers offering customized quantities and purities to meet diverse research needs. Its pricing and sourcing are often influenced by factors such as raw material availability and synthetic route efficiency, topics that dominate procurement-related queries. Additionally, the compound's shelf life and storage conditions—typically in a cool, dry environment under inert atmosphere—are practical considerations for end-users.

Looking ahead, the potential of 1-(naphthalen-2-yl)piperazine in emerging fields like bioconjugation chemistry and targeted drug delivery systems is an area of active investigation. Its compatibility with click chemistry protocols and other modular synthetic strategies positions it as a valuable tool for modern chemical biology. Researchers and industry professionals continue to explore its untapped potential, as evidenced by the steady rise in publications and patents referencing this compound.

In summary, 1-(naphthalen-2-yl)piperazine (CAS No. 57536-91-1) represents a fascinating intersection of organic chemistry, materials science, and pharmaceutical research. Its unique structural features, coupled with its broad applicability, ensure its continued relevance in scientific and industrial contexts. As innovation drives the demand for specialized chemical building blocks, this compound is poised to remain a key player in the development of next-generation technologies and therapeutics.

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