Cas no 148120-37-0 (1-Benzyl-4-(4-nitrobenzyl)piperazine)

1-Benzyl-4-(4-nitrobenzyl)piperazine structure
148120-37-0 structure
Product Name:1-Benzyl-4-(4-nitrobenzyl)piperazine
CAS No:148120-37-0
MF:C18H21N3O2
MW:311.378244161606
MDL:MFCD03725418
CID:232028
PubChem ID:763935
Update Time:2025-07-20

1-Benzyl-4-(4-nitrobenzyl)piperazine Chemical and Physical Properties

Names and Identifiers

    • 1-Benzyl-4-(4-nitrobenzyl)piperazine
    • 1-(4-nitrobenzyl)-4-benzylpiperazine
    • Piperazine,1-[(4-nitrophenyl)methyl]-4-(phenylmethyl)-
    • 4-(4-benzylpiperazinomethyl)-nitrobenzene
    • Piperazine,1-[(4-nitrophenyl)methyl]-4-(phenylmethyl)
    • 1-benzyl-4-[(4-nitrophenyl)Methyl]piperazine
    • 1-Benzyl-4-(4-nitrobenzyl)piperazine95%
    • 1-BENZYL-4-(4-NITROBENZYL)PIPERAZINE 95%
    • MFCD00810765
    • SR-01000201850-1
    • AKOS015839362
    • JSPBNJMOQJJJJH-UHFFFAOYSA-N
    • DTXSID70354123
    • CS-W002699
    • FT-0643419
    • AB00077506-01
    • Cambridge id 5262120
    • SR-01000201850
    • 148120-37-0
    • Piperazine, 1-[(4-nitrophenyl)methyl]-4-(phenylmethyl)-
    • A808737
    • Oprea1_446319
    • SCHEMBL5626457
    • DS-0173
    • SY031405
    • DB-001972
    • MDL： MFCD03725418
    • Inchi： 1S/C18H21N3O2/c22-21(23)18-8-6-17(7-9-18)15-20-12-10-19(11-13-20)14-16-4-2-1-3-5-16/h1-9H,10-15H2
    • InChI Key： JSPBNJMOQJJJJH-UHFFFAOYSA-N
    • SMILES： [O-][N+](C1C=CC(=CC=1)CN1CCN(CC2C=CC=CC=2)CC1)=O

Computed Properties

  • Exact Mass: 311.16300
  • Monoisotopic Mass: 313.179027
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 23
  • Rotatable Bond Count: 5
  • Complexity: 363
  • 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
  • Topological Polar Surface Area: 54.7
  • XLogP3: 2.9

Experimental Properties

  • Color/Form: No data avaiable
  • Density: No data available
  • Melting Point: No data available
  • Boiling Point: 452.4 °C at 760 mmHg
  • Flash Point: 227.4 °C
  • PSA: 52.30000
  • LogP: 3.31160
  • Vapor Pressure: No data available

1-Benzyl-4-(4-nitrobenzyl)piperazine Security Information

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1-Benzyl-4-(4-nitrobenzyl)piperazine Related Literature

Additional information on 1-Benzyl-4-(4-nitrobenzyl)piperazine

Comprehensive Overview of 1-Benzyl-4-(4-nitrobenzyl)piperazine (CAS No. 148120-37-0)

1-Benzyl-4-(4-nitrobenzyl)piperazine, identified by its CAS number 148120-37-0, is a specialized organic compound belonging to the piperazine derivatives family. This compound has garnered significant attention in pharmaceutical and chemical research due to its unique structural properties and potential applications. The presence of both benzyl and nitrobenzyl groups in its molecular framework makes it a versatile intermediate for synthesizing more complex molecules. Researchers and industry professionals often explore its reactivity, stability, and compatibility with other reagents to develop innovative solutions in drug discovery and material science.

In recent years, the demand for piperazine-based compounds like 1-Benzyl-4-(4-nitrobenzyl)piperazine has surged, driven by their role in designing bioactive molecules. Users frequently search for terms such as "piperazine derivatives uses", "nitrobenzyl group applications", and "CAS 148120-37-0 synthesis methods", reflecting the growing interest in this compound. Its structural features, including the electron-withdrawing nitro group and the aromatic benzyl moiety, contribute to its utility in cross-coupling reactions and as a building block for heterocyclic chemistry.

The compound's molecular weight and solubility profile are critical parameters for researchers optimizing reaction conditions. Analytical techniques such as HPLC, NMR spectroscopy, and mass spectrometry are commonly employed to characterize 1-Benzyl-4-(4-nitrobenzyl)piperazine and ensure its purity. Questions like "How to purify 1-Benzyl-4-(4-nitrobenzyl)piperazine?" or "What solvents work best for this compound?" are frequently encountered in forums and academic discussions, highlighting the practical challenges faced by chemists.

From an industrial perspective, 1-Benzyl-4-(4-nitrobenzyl)piperazine is often discussed in the context of green chemistry and sustainable synthesis. With increasing environmental regulations, researchers are exploring eco-friendly methods to produce such compounds without compromising yield or quality. Searches related to "green synthesis of nitrobenzyl derivatives" or "scalable piperazine production" underscore this trend. The compound's stability under various pH conditions and temperatures also makes it a candidate for catalysis studies and process optimization.

Another area of interest is the potential biological activity of 1-Benzyl-4-(4-nitrobenzyl)piperazine. While not a drug itself, its structure is analogous to pharmacologically active molecules targeting central nervous system (CNS) receptors or enzyme inhibitors. Queries like "Does 1-Benzyl-4-(4-nitrobenzyl)piperazine have medicinal properties?" or "Piperazine derivatives in drug design" are common among biomedical researchers. However, rigorous studies are required to validate any therapeutic claims.

In summary, 1-Benzyl-4-(4-nitrobenzyl)piperazine (CAS 148120-37-0) is a multifaceted compound with broad applicability in synthetic chemistry and material science. Its relevance to current research trends, such as sustainable synthesis and bioactive molecule development, ensures its continued prominence in scientific literature. By addressing frequently asked questions and integrating SEO-friendly keywords, this overview aims to serve as a reliable resource for professionals and enthusiasts alike.

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