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3,5-Dichloro-4-hydroxybenzaldehyde

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Identification
Molecular formula
C7H4Cl2O2
CAS number
6282-41-9
IUPAC name
3,5-dichloro-4-hydroxy-benzaldehyde
State
State

At room temperature, 3,5-Dichloro-4-hydroxybenzaldehyde is in a solid state.

Melting point (Celsius)
201.00
Melting point (Kelvin)
474.15
Boiling point (Celsius)
327.00
Boiling point (Kelvin)
600.15
General information
Molecular weight
191.01g/mol
Molar mass
191.0050g/mol
Density
1.5150g/cm3
Appearence

3,5-Dichloro-4-hydroxybenzaldehyde appears as a white to off-white solid. It is typically crystalline in form and may have a slight odor distinctive of benzaldehyde derivatives.

Comment on solubility

Solubility of 3,5-Dichloro-4-hydroxy-benzaldehyde

3,5-Dichloro-4-hydroxy-benzaldehyde, known for its complex structure, exhibits some interesting solubility characteristics:

  • Solvent Compatibility: This compound is generally soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO), making it suitable for various applications in organic synthesis.
  • Water Solubility: The solubility of 3,5-dichloro-4-hydroxy-benzaldehyde in water is limited. This is primarily due to the hydrophobic nature of the aromatic ring, which tends to resist dissolution in polar solvents.
  • Temperature Dependence: As with many organic compounds, increased temperature can enhance solubility. It is advisable to test solubility at different temperatures to find optimal conditions for specific reactions.
  • Hydrogen Bonding: The presence of the −OH group in the structure indicates potential for hydrogen bonding, which may facilitate solubility in certain polar solvents, albeit within a limited scope.

In summary, while 3,5-dichloro-4-hydroxy-benzaldehyde shows good solubility in specific organic solvents, its behavior in aqueous environments is less favorable. Therefore, selection of solvents should consider both compound stability and desired reactivity.

Interesting facts

Interesting Facts about 3,5-Dichloro-4-hydroxy-benzaldehyde

3,5-Dichloro-4-hydroxy-benzaldehyde is a fascinating compound widely recognized in the field of organic chemistry. Here are some intriguing aspects that showcase its importance:

  • Structural Significance: This compound exemplifies the presence of multiple functional groups, including -CHO (aldehyde) and -OH (hydroxyl), attached to a benzene ring. Its chlorine substituents (specifically at the 3 and 5 positions) enhance its reactivity, which makes it a subject of interest in synthetic pathways.
  • Applications in Synthesis: 3,5-Dichloro-4-hydroxy-benzaldehyde serves as a valuable intermediate in organic synthesis. It is frequently used in the preparation of various dye compounds and pharmaceuticals, showcasing its versatility and utility.
  • Biological Activity: Research has indicated that this compound and its derivatives possess biological activities, including antibacterial properties. This makes it a candidate for further studies in the development of therapeutic agents.
  • Innovative Research: Current studies focus on exploring its behavior in different environments, including its potential role in nanotechnology, where it's investigated for creating novel materials with unique properties.
  • Environmental Considerations: As a chlorinated compound, there is an ongoing discussion about its environmental impact and stability. This opens avenues for research on safe disposal and reduction of its ecological footprint.

In summary, 3,5-dichloro-4-hydroxy-benzaldehyde is more than just a chemical formula; it is a platform for innovation and discovery in various scientific disciplines.

Synonyms
3,5-DICHLORO-4-HYDROXYBENZALDEHYDE
DTXSID20177708
NSC 31590
DTXCID40100199
823-616-9
liygcljythrbqv-uhfffaoysa-n
2314-36-5
Benzaldehyde, 3,5-dichloro-4-hydroxy-
MFCD00017605
3,5-Dichloro-4-hydroxy-benzaldehyde
Benzaldehyde, 3,?5-?dichloro-?4-?hydroxy-
Benzaldehyde,3,5-dichloro-4-hydroxy-
NSC31590
SCHEMBL574999
Benzaldehyde,5-dichloro-4-hydroxy-
NSC-31590
STK198692
AKOS000291227
CS-W006820
FD70957
NCGC00340803-01
1-formyl-3,5-dichloro-4-hydroxy-benzene
DS-16729
SY018866
3,5-dichloro-4-hydroxybenzaldehyde, AldrichCPR
EN300-307613
AB01333405-02
AH-487/13096001
Z57313907