Cas no 2751615-89-9 (1-(2-Methylphenyl)-4-nitrosopiperazine)

1-(2-Methylphenyl)-4-nitrosopiperazine is a nitrosated piperazine derivative with potential applications in organic synthesis and pharmaceutical research. Its structure features a 2-methylphenyl group attached to a nitrosopiperazine core, offering reactivity useful for further functionalization or as an intermediate in heterocyclic chemistry. The nitroso group provides a versatile handle for nucleophilic or electrophilic transformations, while the aromatic methyl substituent may influence solubility and steric properties. This compound is of interest in medicinal chemistry due to the pharmacological relevance of nitrosopiperazine scaffolds. Proper handling is advised, as nitroso compounds can exhibit sensitivity to light and heat. Storage under inert conditions is recommended to maintain stability.
1-(2-Methylphenyl)-4-nitrosopiperazine structure
2751615-89-9 structure
Product Name:1-(2-Methylphenyl)-4-nitrosopiperazine
CAS No:2751615-89-9
MF:C11H15N3O
MW:205.256302118301
MDL:MFCD34594861
CID:5666066
PubChem ID:165739385
Update Time:2025-05-20

1-(2-Methylphenyl)-4-nitrosopiperazine Chemical and Physical Properties

Names and Identifiers

    • EN300-27716389
    • 1-(2-methylphenyl)-4-nitrosopiperazine
    • 2751615-89-9
    • 1-(2-Methylphenyl)-4-nitrosopiperazine
    • MDL: MFCD34594861
    • Inchi: 1S/C11H15N3O/c1-10-4-2-3-5-11(10)13-6-8-14(12-15)9-7-13/h2-5H,6-9H2,1H3
    • InChI Key: IMIQCBFBCSYVHH-UHFFFAOYSA-N
    • SMILES: O=NN1CCN(C2C=CC=CC=2C)CC1

Computed Properties

  • Exact Mass: 205.121512110g/mol
  • Monoisotopic Mass: 205.121512110g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 1
  • Complexity: 214
  • 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: 2.6
  • Topological Polar Surface Area: 35.9?2

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Additional information on 1-(2-Methylphenyl)-4-nitrosopiperazine

Comprehensive Analysis of 1-(2-Methylphenyl)-4-nitrosopiperazine (CAS No. 2751615-89-9): Properties, Applications, and Research Insights

The compound 1-(2-Methylphenyl)-4-nitrosopiperazine (CAS No. 2751615-89-9) is a specialized organic molecule that has garnered significant attention in pharmaceutical and chemical research. With its unique structural features, including a nitrosopiperazine moiety and a 2-methylphenyl substituent, this compound serves as a valuable intermediate in the synthesis of bioactive molecules. Researchers are increasingly exploring its potential in drug discovery, particularly in targeting enzyme modulation and signal transduction pathways.

In recent years, the demand for nitrosopiperazine derivatives has surged due to their role in developing novel therapeutic agents. A 2023 study highlighted the compound’s relevance in designing inhibitors for neurodegenerative diseases, aligning with the growing public interest in brain health supplements and cognitive enhancers. This connection to trending health topics enhances its visibility in SEO-driven searches, as users frequently query terms like "nitrosopiperazine benefits" or "2-methylphenyl compounds in medicine."

The physicochemical properties of 1-(2-Methylphenyl)-4-nitrosopiperazine further underscore its versatility. Its moderate solubility in organic solvents and stability under controlled conditions make it suitable for high-throughput screening and combinatorial chemistry. Laboratories prioritize its use in structure-activity relationship (SAR) studies, a topic frequently searched by chemistry students and professionals alike.

From an industrial perspective, the compound’s synthesis involves green chemistry principles, addressing the global push for sustainable chemical processes. Optimized routes using catalytic nitrosation reduce waste generation, resonating with environmentally conscious audiences. This aligns with popular search queries such as "eco-friendly nitrosamine synthesis" and "green chemistry innovations 2024."

Ongoing research explores the 1-(2-Methylphenyl)-4-nitrosopiperazine’s potential in cancer immunotherapy, a hotspot in medical science. Preliminary data suggest its ability to modulate immune checkpoints, a feature highly searched under terms like "small molecule immunotherapeutics." Such applications position it as a candidate for next-generation oncology drugs, further driving academic and commercial interest.

Quality control protocols for CAS No. 2751615-89-9 emphasize HPLC purity validation and spectroscopic characterization (NMR, MS), ensuring reproducibility—a critical factor for laboratories adhering to Good Manufacturing Practices (GMP). These technical aspects frequently appear in searches related to "analytical chemistry standards" and "pharmaceutical compound certification."

In conclusion, 1-(2-Methylphenyl)-4-nitrosopiperazine represents a nexus of innovation across multiple disciplines. Its intersection with trending topics like precision medicine, sustainability, and drug development ensures its continued relevance in both scientific literature and search engine algorithms. Future studies may unlock further applications, solidifying its role in advancing life sciences and material chemistry.

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