Cas no 2751615-89-9 (1-(2-Methylphenyl)-4-nitrosopiperazine)
1-(2-Methylphenyl)-4-nitrosopiperazine Chemical and Physical Properties
Names and Identifiers
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- EN300-27716389
- 1-(2-methylphenyl)-4-nitrosopiperazine
- 2751615-89-9
- 1-(2-Methylphenyl)-4-nitrosopiperazine
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- 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
1-(2-Methylphenyl)-4-nitrosopiperazine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-27716389-0.05g |
1-(2-methylphenyl)-4-nitrosopiperazine |
2751615-89-9 | 95.0% | 0.05g |
$229.0 | 2025-03-20 | |
| Enamine | EN300-27716389-0.1g |
1-(2-methylphenyl)-4-nitrosopiperazine |
2751615-89-9 | 95.0% | 0.1g |
$342.0 | 2025-03-20 | |
| Enamine | EN300-27716389-0.25g |
1-(2-methylphenyl)-4-nitrosopiperazine |
2751615-89-9 | 95.0% | 0.25g |
$487.0 | 2025-03-20 | |
| Enamine | EN300-27716389-0.5g |
1-(2-methylphenyl)-4-nitrosopiperazine |
2751615-89-9 | 95.0% | 0.5g |
$768.0 | 2025-03-20 | |
| Enamine | EN300-27716389-1.0g |
1-(2-methylphenyl)-4-nitrosopiperazine |
2751615-89-9 | 95.0% | 1.0g |
$986.0 | 2025-03-20 | |
| Enamine | EN300-27716389-2.5g |
1-(2-methylphenyl)-4-nitrosopiperazine |
2751615-89-9 | 95.0% | 2.5g |
$1931.0 | 2025-03-20 | |
| Enamine | EN300-27716389-5.0g |
1-(2-methylphenyl)-4-nitrosopiperazine |
2751615-89-9 | 95.0% | 5.0g |
$2858.0 | 2025-03-20 | |
| Enamine | EN300-27716389-10.0g |
1-(2-methylphenyl)-4-nitrosopiperazine |
2751615-89-9 | 95.0% | 10.0g |
$4236.0 | 2025-03-20 | |
| Enamine | EN300-27716389-1g |
1-(2-methylphenyl)-4-nitrosopiperazine |
2751615-89-9 | 95% | 1g |
$986.0 | 2023-09-10 | |
| Enamine | EN300-27716389-5g |
1-(2-methylphenyl)-4-nitrosopiperazine |
2751615-89-9 | 95% | 5g |
$2858.0 | 2023-09-10 |
1-(2-Methylphenyl)-4-nitrosopiperazine Related Literature
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Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
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Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
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Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
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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