Skip to main content

2-Nitrophenanthrene

ADVERTISEMENT
Identification
Molecular formula
C14H9NO2
CAS number
1510-83-0
IUPAC name
2-nitrophenanthrene
State
State

At room temperature, 2-nitrophenanthrene is typically in a solid state. It retains its aromatic compound characteristics, contributing to its stability as a solid under standard conditions.

Melting point (Celsius)
102.00
Melting point (Kelvin)
375.20
Boiling point (Celsius)
438.40
Boiling point (Kelvin)
711.60
General information
Molecular weight
223.22g/mol
Molar mass
223.2210g/mol
Density
1.3900g/cm3
Appearence

2-Nitrophenanthrene is commonly found as a yellow crystalline solid. Its crystalline structure can often appear with a bright or dull yellow hue, depending on particle size and purity.

Comment on solubility

Solubility of 2-nitrophenanthrene

2-Nitrophenanthrene, with the chemical formula C14H9NO2, exhibits interesting solubility characteristics that can vary based on the solvent used. Generally, it is known to be:

  • Moderately soluble in organic solvents such as ethanol and acetone.
  • Less soluble in water due to its hydrophobic phenanthrene backbone and the presence of a nitro group.
  • Practically insoluble in non-polar solvents like hexane.

This solubility behavior can be attributed to the polarity of 2-nitrophenanthrene and its interactions with other molecules. When considering solubility, one might remember the essential rule of thumb in chemistry: "Like dissolves like." Thus, 2-nitrophenanthrene, being a largely non-polar compound, interacts better with non-polar or slightly polar solvents, rather than completely polar solvents such as water.

In summary, the solubility of 2-nitrophenanthrene is influenced by its structure and the types of solvents used, making it an interesting compound to study in varied chemical contexts.

Interesting facts

Interesting Facts about 2-Nitrophenanthrene

2-Nitrophenanthrene, a fascinating organic compound, belongs to the family of nitrogen-containing polycyclic aromatic hydrocarbons. Here's what makes it particularly noteworthy:

  • Structure and Isomerism: This compound features a nitro group (-NO2) positioned on the phenanthrene framework. The specific placement of the nitro group leads to distinct chemical properties and behaviors, especially under various conditions.
  • Applications in Research: 2-Nitrophenanthrene has garnered attention in the field of organic chemistry, particularly in studies related to polycyclic aromatic hydrocarbons (PAHs). Its derivatives are often explored for their usefulness in synthesizing advanced materials and in research involving environmental science.
  • Environmental Impact: Like many PAHs, 2-nitrophenanthrene poses potential environmental concerns. It can be a byproduct of combustion processes and is subject to study regarding its behavior in the atmosphere, as well as its implications for soil and water contamination.
  • Photochemical Properties: The compound exhibits interesting photochemical characteristics, which can be explored for their potential in photodynamic therapy and other applications focusing on light-induced reactions.
  • Safety Precautions: When handling 2-nitrophenanthrene, it is crucial to follow safety protocols as it can be harmful. Proper protective measures should be taken to avoid inhalation or skin contact, highlighting the importance of safety in the lab.

In summary, 2-nitrophenanthrene stands out due to its intriguing structure, diverse applications, and implications in both research and environmental science. Its role in understanding the nuances of nitrogen-substituted aromatic compounds continues to capture the interest of chemists and environmental scientists alike.

Synonyms
2-NITROPHENANTHRENE
Phenanthrene, 2-nitro-
CCRIS 3370
PKF8VDC4N7
3-Nitrophenathrene
BRN 2372743
DTXSID70168823
4-05-00-02304 (Beilstein Handbook Reference)
DTXCID4091314
PYZVVHPEDWRKME-UHFFFAOYSA-N
17024-18-9
2-Nitro-phenanthrene
Phenanthrene,2-nitro-
2-Nitro-phenanthren
UNII-PKF8VDC4N7
CHEMBL354694
SCHEMBL1527627
SCHEMBL6416195
SCHEMBL10574947
DB-217512