Cas no 40257-56-5 (Benzenamine, 2-nitro-4-(4-nitrophenoxy)-)

Benzenamine, 2-nitro-4-(4-nitrophenoxy)-, is a nitro-substituted aromatic amine with a phenoxy linkage, offering distinct chemical properties for specialized applications. Its structure, featuring two nitro groups and an ether bridge, enhances reactivity in electrophilic and nucleophilic substitution reactions, making it valuable as an intermediate in organic synthesis. The compound's electron-withdrawing nitro groups contribute to its stability and utility in the preparation of dyes, pharmaceuticals, and agrochemicals. Its well-defined molecular architecture allows for precise functionalization, facilitating the development of complex derivatives. The compound is typically handled under controlled conditions due to its potential sensitivity to heat and light.
Benzenamine, 2-nitro-4-(4-nitrophenoxy)- structure
40257-56-5 structure
Product Name:Benzenamine, 2-nitro-4-(4-nitrophenoxy)-
CAS No:40257-56-5
MF:C12H9N3O5
MW:275.216962575912
CID:324455
PubChem ID:12032722
Update Time:2025-06-15

Benzenamine, 2-nitro-4-(4-nitrophenoxy)- Chemical and Physical Properties

Names and Identifiers

    • Benzenamine, 2-nitro-4-(4-nitrophenoxy)-
    • 2-nitro-4-(4-nitrophenoxy)aniline
    • DTXSID80476209
    • 4-(4-Nitrophenoxy)-2-nitroaniline
    • SCHEMBL554702
    • Benzenamine,2-nitro-4-(4-nitrophenoxy)-
    • F18169
    • CFIDSVMFMCEQOP-UHFFFAOYSA-N
    • 40257-56-5
    • Inchi: 1S/C12H9N3O5/c13-11-6-5-10(7-12(11)15(18)19)20-9-3-1-8(2-4-9)14(16)17/h1-7H,13H2
    • InChI Key: CFIDSVMFMCEQOP-UHFFFAOYSA-N
    • SMILES: O(C1C=CC(=CC=1)[N+](=O)[O-])C1=CC=C(C(=C1)[N+](=O)[O-])N

Computed Properties

  • Exact Mass: 275.05422040g/mol
  • Monoisotopic Mass: 275.05422040g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 2
  • Complexity: 359
  • 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: 3.2
  • Topological Polar Surface Area: 127?2

Benzenamine, 2-nitro-4-(4-nitrophenoxy)- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1735321-1g
2-Nitro-4-(4-nitrophenoxy)aniline
40257-56-5 98%
1g
¥4977.00 2024-05-15

Additional information on Benzenamine, 2-nitro-4-(4-nitrophenoxy)-

Benzenamine, 2-nitro-4-(4-nitrophenoxy)- (CAS No. 40257-56-5): A Comprehensive Overview

Benzenamine, 2-nitro-4-(4-nitrophenoxy)- (CAS No. 40257-56-5) is a versatile compound with significant applications in the fields of chemistry, biology, and pharmaceuticals. This aromatic amine derivative is characterized by its unique structural features, which include a nitro group and a nitrophenoxy substituent. These functional groups endow the compound with a range of chemical and biological properties that make it an important molecule for both academic research and industrial applications.

The chemical structure of Benzenamine, 2-nitro-4-(4-nitrophenoxy)- consists of a benzene ring substituted with an amino group at the 1-position, a nitro group at the 2-position, and a nitrophenoxy group at the 4-position. The presence of these substituents imparts specific reactivity and stability to the molecule, making it suitable for various synthetic transformations and biological assays.

In recent years, significant advancements have been made in understanding the properties and applications of Benzenamine, 2-nitro-4-(4-nitrophenoxy)-. One notable area of research is its use as an intermediate in the synthesis of pharmaceuticals. The compound's ability to undergo selective functionalization reactions makes it a valuable starting material for the production of drugs targeting various diseases. For instance, studies have shown that derivatives of this compound exhibit potent anti-inflammatory and anti-cancer activities, making them promising candidates for drug development.

Another important application of Benzenamine, 2-nitro-4-(4-nitrophenoxy)- is in the field of materials science. The compound can be used to synthesize polymers with unique optical and electronic properties. These polymers have potential applications in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The ability to fine-tune the electronic properties of these materials through molecular design has opened up new avenues for developing advanced electronic devices.

The environmental impact of Benzenamine, 2-nitro-4-(4-nitrophenoxy)- is also an area of ongoing research. Studies have focused on understanding its biodegradability and potential ecotoxicological effects. Preliminary results suggest that the compound is relatively stable under environmental conditions but can be degraded by specific microbial consortia. This information is crucial for assessing the environmental safety of products containing this compound.

In addition to its synthetic and material science applications, Benzenamine, 2-nitro-4-(4-nitrophenoxy)- has been studied for its potential use in analytical chemistry. The compound's unique spectral properties make it a useful probe for various analytical techniques, including UV-Vis spectroscopy and mass spectrometry. These techniques are essential for characterizing complex mixtures and monitoring chemical reactions in real-time.

The safety profile of Benzenamine, 2-nitro-4-(4-nitrophenoxy)- is another critical aspect that has been extensively investigated. While the compound is generally considered safe when handled properly, it is important to follow standard laboratory safety protocols to minimize any potential risks. This includes using appropriate personal protective equipment (PPE) and ensuring proper ventilation in laboratory settings.

In conclusion, Benzenamine, 2-nitro-4-(4-nitrophenoxy)- (CAS No. 40257-56-5) is a multifaceted compound with a wide range of applications in chemistry, biology, pharmaceuticals, materials science, and analytical chemistry. Its unique structural features and versatile reactivity make it an invaluable molecule for both academic research and industrial processes. As research continues to advance, it is likely that new applications and insights into the properties of this compound will emerge, further solidifying its importance in the scientific community.

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