Cas no 607-44-3 (2-NAPHTHALENAMINE, 5-NITRO-)
2-NAPHTHALENAMINE, 5-NITRO- Chemical and Physical Properties
Names and Identifiers
-
- 2-NAPHTHALENAMINE, 5-NITRO-
- 5-Nitro-2-naphthalenamine
- 5-nitro-2-naphthylamine
- NoName_3398
- F70885
- SCHEMBL8686915
- 5-nitronaphthalen-2-amine
- 607-44-3
- 5-Nitro-2-naphthalenamine #
- DTXSID60902834
- AKOS006272071
- naphthalene, 2-amino-5-nitro-
- PPYFMWXMDIAZSV-UHFFFAOYSA-N
- 1-Nitro-6-aminonaphthalene
- AE-562/12222170
-
- Inchi: 1S/C10H8N2O2/c11-8-4-5-9-7(6-8)2-1-3-10(9)12(13)14/h1-6H,11H2
- InChI Key: PPYFMWXMDIAZSV-UHFFFAOYSA-N
- SMILES: [O-][N+](C1C=CC=C2C=C(C=CC2=1)N)=O
Computed Properties
- Exact Mass: 188.058577502Da
- Monoisotopic Mass: 188.058577502Da
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 14
- Rotatable Bond Count: 0
- Complexity: 227
- 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: 2.5
- Topological Polar Surface Area: 71.8?2
2-NAPHTHALENAMINE, 5-NITRO- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A219006572-1g |
5-Nitronaphthalen-2-amine |
607-44-3 | 95% | 1g |
$1450.00 | 2023-09-01 |
2-NAPHTHALENAMINE, 5-NITRO- Related Literature
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Tanya Ostapenko,Peter J. Collings,Samuel N. Sprunt,J. T. Gleeson Soft Matter, 2013,9, 9487-9498
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2. An integrated chip for immunofluorescence and its application to analyze lysosomal storage disordersJie Shen,Ying Zhou,Tu Lu,Junya Peng,Zhixiang Lin,Yuhong Pang,Li Yu Lab Chip, 2012,12, 317-324
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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Kui Wu,Zhihua Yang,Shilie Pan Dalton Trans., 2015,44, 19856-19864
Additional information on 2-NAPHTHALENAMINE, 5-NITRO-
Recent Advances in the Study of 2-NAPHTHALENAMINE, 5-NITRO- (CAS: 607-44-3) in Chemical and Biomedical Research
The compound 2-NAPHTHALENAMINE, 5-NITRO- (CAS: 607-44-3) has garnered significant attention in recent years due to its potential applications in chemical synthesis and biomedical research. This aromatic amine, characterized by a nitro group at the 5-position of the naphthalene ring, has been investigated for its role as an intermediate in the synthesis of dyes, pharmaceuticals, and other fine chemicals. Recent studies have also explored its biological activities, including its potential as a precursor for novel therapeutic agents.
One of the key areas of research involving 2-NAPHTHALENAMINE, 5-NITRO- is its use in the development of azo dyes. Azo dyes are widely used in the textile, food, and pharmaceutical industries, and the nitro-substituted naphthalene derivatives are known for their vibrant colors and stability. Recent advancements in synthetic chemistry have optimized the production processes for these dyes, reducing environmental impact while maintaining high yields. Additionally, the compound's role in the synthesis of more complex aromatic systems has been highlighted in several studies, demonstrating its versatility as a building block in organic chemistry.
In the biomedical field, 2-NAPHTHALENAMINE, 5-NITRO- has been studied for its potential pharmacological properties. Research has shown that derivatives of this compound exhibit promising antimicrobial and anti-inflammatory activities. For instance, a 2023 study published in the *Journal of Medicinal Chemistry* reported the synthesis of novel nitro-naphthalene derivatives with significant activity against drug-resistant bacterial strains. These findings suggest that 2-NAPHTHALENAMINE, 5-NITRO- could serve as a valuable scaffold for the development of new antibiotics.
Another notable application of 2-NAPHTHALENAMINE, 5-NITRO- is in the field of cancer research. Recent investigations have explored its potential as a precursor for anticancer agents. A study conducted by researchers at the National Cancer Institute demonstrated that certain nitro-naphthalene derivatives could inhibit the growth of tumor cells by targeting specific metabolic pathways. These results, while preliminary, underscore the compound's potential in oncology drug development.
Despite its promising applications, the use of 2-NAPHTHALENAMINE, 5-NITRO- is not without challenges. The compound's nitro group can contribute to toxicity, raising concerns about its safety in pharmaceutical applications. Recent research has focused on modifying the chemical structure to reduce toxicity while retaining biological activity. For example, a 2024 study proposed the use of prodrug strategies to mitigate the adverse effects associated with nitro-aromatic compounds, opening new avenues for safer drug design.
In conclusion, 2-NAPHTHALENAMINE, 5-NITRO- (CAS: 607-44-3) continues to be a compound of significant interest in both chemical and biomedical research. Its versatility as a synthetic intermediate and its potential pharmacological activities make it a valuable subject for ongoing studies. Future research should focus on optimizing its properties for safer and more effective applications, particularly in the development of new therapeutic agents.
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