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3-Nitroanisole

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Identification
Molecular formula
C7H7NO3
CAS number
555-02-8
IUPAC name
1-methoxy-3-nitro-benzene
State
State

3-Nitroanisole is in the liquid state at room temperature.

Melting point (Celsius)
6.00
Melting point (Kelvin)
279.00
Boiling point (Celsius)
245.00
Boiling point (Kelvin)
518.00
General information
Molecular weight
153.14g/mol
Molar mass
153.1370g/mol
Density
1.1820g/cm3
Appearence

3-Nitroanisole is a pale yellow liquid.

Comment on solubility

Solubility of 1-Methoxy-3-nitro-benzene

1-Methoxy-3-nitro-benzene, also known as meta-nitroanisol, exhibits unique solubility characteristics that are influenced by its molecular structure. This compound is an aromatic ether with both a methoxy group and a nitro group, which play significant roles in its solubility.

When discussing its solubility, several key points can be noted:

  • Polar vs Nonpolar Solvents: 1-Methoxy-3-nitro-benzene is generally more soluble in polar organic solvents such as methanol, ethanol, and acetone. This is due to the presence of the methoxy group, which increases its polarity.

  • Insolubility in Water: This compound is practically insoluble in water. The nonpolar aromatic ring does not interact well with water molecules, which are polar.

  • Solvent Interactions: In polar solvents, the nitro group can engage in hydrogen bonding, further enhancing solubility. However, in nonpolar solvents, the solubility decreases significantly.

Overall, the solubility of 1-methoxy-3-nitro-benzene is a fascinating reflection of how functional groups influence interaction with different solvents. As a reminder, "like dissolves like," meaning polar compounds tend to dissolve well in polar solvents, while nonpolar compounds are better suited for nonpolar environments.

Interesting facts

Interesting Facts about 1-Methoxy-3-nitro-benzene

1-Methoxy-3-nitro-benzene, also known as 3-Nitroanisol, is a fascinating compound that belongs to the class of nitro compounds. It is widely studied for its applications in both industrial and academic settings. Here are some intriguing aspects of this compound:

  • Precursor for Synthesis: 1-Methoxy-3-nitro-benzene serves as an important intermediate in the synthesis of various pharmaceutical compounds and agrochemicals, facilitating the development of novel therapeutics.
  • Electrophilic Aromatic Substitution: The presence of both methoxy and nitro groups on the benzene ring influences reactivity, making it a valuable substrate for electrophilic aromatic substitution reactions.
  • Environmental Considerations: As part of the nitro compound family, this compound is studied for its environmental impact and potential degradation pathways, thus contributing to the field of environmental chemistry.
  • Characterization Techniques: Researchers often employ diverse characterization techniques, such as NMR and IR spectroscopy, to study the structure and properties of this compound, revealing insights into its molecular behavior.

By investigating 1-Methoxy-3-nitro-benzene, scientists can enhance our understanding of organic chemistry, the nature of electrophilic reactions, and the importance of nitro compounds in drug development and environmental applications.


Synonyms
3-Nitroanisole
1-Methoxy-3-nitrobenzene
555-03-3
M-NITROANISOLE
m-Methoxynitrobenzene
3-Methoxynitrobenzene
Benzene, 1-methoxy-3-nitro-
Anisole, m-nitro-
Methyl m-nitrophenyl ether
NSC 4956
CCRIS 2320
3-nitroanisol
EINECS 209-079-8
UNII-V9920UY61E
V9920UY61E
NSC-4956
3-NITROMETHOXYBENZENE
M-NITROANISOLE [MI]
DTXSID3060295
CHEBI:48972
3-METHOXY-1-NITROBENZENE
Anisole, m-nitro-(8CI)
DTXCID3041900
209-079-8
inchi=1/c7h7no3/c1-11-7-4-2-3-6(5-7)8(9)10/h2-5h,1h
wgyfinwerlnphr-uhfffaoysa-n
1-methoxy-3-nitro-benzene
3-nitro-anisole
m-Nitroanisol
NSC4956
MFCD00007237
3-Nitroanisole, 99%
SCHEMBL515302
Methyl,hydroxy(4-nitrophenyl)-
AKOS015916731
FS-4700
DB-052746
DB-265511
N0124
NS00033328
D91642
A830679
Q27121414