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2-Amino-3-nitronaphthalene

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Identification
Molecular formula
C10H8N2O2
CAS number
602-96-0
IUPAC name
3-nitronaphthalen-2-amine
State
State

At room temperature, 2-Amino-3-nitronaphthalene exists as a solid. It is used mainly in research and applications involving nitro compounds and requires specific handling due to its potential hazardous effects.

Melting point (Celsius)
168.00
Melting point (Kelvin)
441.15
Boiling point (Celsius)
356.00
Boiling point (Kelvin)
629.15
General information
Molecular weight
188.18g/mol
Molar mass
188.1840g/mol
Density
1.4012g/cm3
Appearence

2-Amino-3-nitronaphthalene typically appears as a yellow to light brown crystalline powder. It is solid at room temperature and is notable for its stability as a nitroaromatic compound. Care must be taken in handling as it may be harmful.

Comment on solubility

Solubility of 3-nitronaphthalen-2-amine (C10H8N2O2)

3-nitronaphthalen-2-amine, a compound with a unique structure, exhibits notable solubility properties that are essential for its applications in various fields. Understanding its solubility can help in predicting its behavior in different environments. Here are some key points regarding its solubility:

  • Polar and Non-Polar Solvents: This compound is known to be more soluble in organic solvents compared to water, due to its aromatic structure which promotes interactions with non-polar solvent molecules.
  • Hydrogen Bonding: Although it has some polar functional groups, the ability to form hydrogen bonds can lead to moderate solubility in polar solvents.
  • Temperature Dependence: Solubility can vary with temperature, where increased temperatures may enhance the solubility of the compound in certain solvents.
  • pH Sensitivity: The solubility of amine compounds can be influenced by the pH of the solution, becoming more soluble in acidic conditions.

In conclusion, while 3-nitronaphthalen-2-amine shows a preference for non-polar solvents, it can also demonstrate solubility in polar environments under certain conditions. Understanding these factors is crucial for its usage in chemical synthesis and analysis.

Interesting facts

Interesting Facts about 3-Nitronaphthalen-2-amine

3-Nitronaphthalen-2-amine, a derivative of naphthalene, presents a fascinating profile that captures the attention of chemists and industrial scientists alike. This compound is noteworthy for several reasons:

  • Structure and Stability: The presence of both nitro and amino functional groups in its structure contributes to its stability and makes it an interesting target for synthetic variations.
  • Applications: 3-Nitronaphthalen-2-amine is primarily used in dye manufacturing, particularly in producing azo dyes, which are famous for their vibrant colors.
  • Synthetic Relevance: This compound can serve as a precursor in various organic synthesis reactions, allowing chemists to explore a range of chemical transformations.
  • Environmental Impact: Compounds like 3-nitronaphthalen-2-amine are part of a larger discussion on environmental chemistry and toxicity. The proper handling and disposal of such compounds are crucial to mitigate their ecological footprint.

Noteworthy is the classification of this compound as a potential environmental pollutant, prompting research on its behavior in various ecosystems. Researchers have noted that compounds similar to 3-nitronaphthalen-2-amine can lead to bioaccumulation and toxicity in aquatic organisms.

As one delves deeper into its chemical properties, an intriguing quote by a prominent chemist comes to mind: "The beauty of chemistry lies in the connections we create through compounds and the stories they tell." This sentiment rings true in understanding the significance of 3-nitronaphthalen-2-amine within the broader field of chemical research.

Synonyms
3-nitronaphthalen-2-amine
3-Nitro-2-naphthylamine
13115-28-1
2-NAPHTHYLAMINE, 3-NITRO-
2-Amino-3-nitronaphthalene
BRN 2103185
3-nitro-2-naphthalenamine
2-Naphthalenamine, 3-nitro-
9AQ5CXG6T2
Nitro-2-naphthylamine, 3-
4-12-00-03185 (Beilstein Handbook Reference)
CHEMBL84041
SCHEMBL8686891
naphthalene, 2-amino-3-nitro-
SCHEMBL10347267
DTXSID60156916
SBB090758
AKOS006272349
DB-366566