Skip to main content

2-Nitrobenzaldehyde

ADVERTISEMENT
Identification
Molecular formula
C7H5NO3
CAS number
552-89-6
IUPAC name
2-nitrobenzaldehyde
State
State

At room temperature, 2-nitrobenzaldehyde is in a solid state. It is quite stable under normal conditions but should be stored appropriately to avoid moisture and excessive heat.

Melting point (Celsius)
42.00
Melting point (Kelvin)
315.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
151.12g/mol
Molar mass
151.1230g/mol
Density
1.3560g/cm3
Appearence

2-Nitrobenzaldehyde is typically a pale yellow crystalline solid. Its crystals are quite fine and can often appear powdery upon settling. It can exhibit a slight odor characteristic of aromatic compounds.

Comment on solubility

Solubility of 2-nitrobenzaldehyde

2-nitrobenzaldehyde, with the chemical formula C7H5NO2, exhibits interesting solubility characteristics that are essential for its applications in various chemical reactions and synthesis processes.

Solubility Characteristics

  • Solvent Compatibility: It is generally soluble in organic solvents such as ethanol, acetone, and dichloromethane. However, it has low solubility in water.
  • Polarity Influence: The presence of the nitro group (-NO2) contributes to its polarity, which affects its solubility profile in different solvents.
  • Temperature Dependency: The solubility of 2-nitrobenzaldehyde can increase with temperature, making hotter solvents more effective for dissolving this compound.

In summary, the solubility of 2-nitrobenzaldehyde is influenced by various factors including polarity, the choice of solvent, and temperature. It's essential to consider these factors when using this compound in laboratory or industrial settings.

Interesting facts

Interesting Facts about 2-Nitrobenzaldehyde

2-Nitrobenzaldehyde is a fascinating organic compound that belongs to the family of nitro-substituted aromatic aldehydes. It is not only an important compound in organic synthesis but also serves as a valuable building block in the creation of various chemicals.

Key Attributes

  • Structure: The compound features a nitro group (-NO2) attached to the second position of the benzaldehyde ring, which influences its reactivity and properties.
  • Synthesis: It can be synthesized through the nitration of benzaldehyde, showcasing the versatility and adaptability of classical organic chemistry techniques. This method typically allows for regioselective substitution.
  • Applications: 2-Nitrobenzaldehyde is widely used in:
    • Organic synthesis as an intermediate for pharmaceuticals.
    • The production of dyes and pigments, where its vivid color enhances the visual appeal.
    • The development of pesticides and agrochemicals, showcasing its importance in agricultural science.

Health and Safety Considerations

As with many chemical compounds, it is essential to handle 2-nitrobenzaldehyde with care. Here are some considerations:

  • Hazards: It can be irritating to the skin and eyes, and inhalation or ingestion should be avoided.
  • Protective Measures: Proper protective equipment such as gloves and goggles should always be worn when working with this compound.

In Summary

2-Nitrobenzaldehyde is a remarkable compound that bridges various fields of chemistry, from synthetic organic chemistry to industrial applications. Its unique properties and reactivity make it a compound of interest for both research and practical applications. As a chemist, understanding the roles and reactions of compounds like 2-nitrobenzaldehyde enriches our knowledge of organic chemistry and fuels innovation across multiple disciplines.

Synonyms
2-NITROBENZALDEHYDE
o-Nitrobenzaldehyde
Benzaldehyde, 2-nitro-
Benzaldehyde, o-nitro-
2-Nitro-benzaldehyde
ortho-nitrobenzaldehyde
CCRIS 2322
NSC 5713
EINECS 209-025-3
DTXSID0022060
CHEBI:66927
AI3-02415
48B18Q9B8E
2-formyl-3-nitrobenzene
NSC-5713
NITROBENZALDEHYDE, 2-
UNII-48B18Q9B8E
CCRIS-2322
DTXCID002060
1-FORMYL-2-NITROBENZENE
EC 209-025-3
oNitrobenzaldehyde
Benzaldehyde, onitro
Benzaldehyde, 2nitro
2-NITROBENZENECARBOXALDEHYDE
209-025-3
cmwkitsntdaedt-uhfffaoysa-n
inchi=1/c7h5no3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-5
552-89-6
Nitrobenzaldehyde
nitro benzaldehyde
MFCD00007132
2-FORMYLNITROBENZENE
nitrobenzaldehye
o-nitrobenzaldehyd
2-nitrobezaldehyde
2-nitrobenzaldehvde
orthonitrobenzaldehyde
o-nitrobenz- aldehyde
Benzaldehyde 2-nitro-
2-Nitrobenzaldehyde, 98%
SCHEMBL5654
2-Nitrobenzenecarboxyaldehyde
2-Nitrobenzaldehyde, 99.0%
CHEMBL166559
SCHEMBL18896991
NSC5713
STR01350
Tox21_202929
BBL023492
CX1109
STL185565
AKOS000118969
AKOS025395656
CS-W007454
FN37099
HY-W007454
PS-5294
NCGC00260475-01
BP-10099
CAS-552-89-6
SY001405
DB-024130
N0130
NS00006033
EN300-18099
AH-214/25003638
Q1055849
Z57162107
F1294-0142