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Dichlorovanillin

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Identification
Molecular formula
C8H6Cl2O3
CAS number
6330-01-6
IUPAC name
2,3-dichloro-4-hydroxy-5-methoxy-benzaldehyde
State
State

Dichlorovanillin is primarily found in a solid state at room temperature, appearing as a crystalline powder.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
304.00
Boiling point (Kelvin)
577.15
General information
Molecular weight
221.04g/mol
Molar mass
221.0420g/mol
Density
1.4860g/cm3
Appearence

Dichlorovanillin typically appears as a white to light yellow crystalline solid. The compound may exhibit a slight brownish tint depending on its purity. It is often found in powdered form for use in various applications.

Comment on solubility

Solubility of 2,3-Dichloro-4-hydroxy-5-methoxy-benzaldehyde

The compound 2,3-dichloro-4-hydroxy-5-methoxy-benzaldehyde, with its complex structure, displays interesting solubility characteristics. While specific solubility data may not always be available, the following observations can be made:

  • Polarity: This compound contains both chlorine and hydroxyl groups, contributing to its overall polarity. The presence of these polar functional groups typically enhances solubility in polar solvents.
  • Solvent Compatibility: It is likely to be more soluble in polar solvents such as methanol and water, while being less soluble in non-polar solvents like hexane.
  • Hydrogen Bonding: The hydroxyl group allows for potential hydrogen bonding, which can further increase solubility in polar environments.

In summary, solubility in polar solvents can be expected, with the compound showing limited solubility in non-polar solvents. As a general rule, compounds with multiple polar functional groups tend to exhibit enhanced solubility in polar solvents, aligning well with the properties of 2,3-dichloro-4-hydroxy-5-methoxy-benzaldehyde.

Interesting facts

Interesting Facts about 2,3-Dichloro-4-hydroxy-5-methoxy-benzaldehyde

2,3-Dichloro-4-hydroxy-5-methoxy-benzaldehyde, a fascinating compound in the realm of organic chemistry, is known for its unique structural features and diverse applications. Here are some intriguing aspects:

  • Chlorine Substituents: This compound contains two chlorine atoms which significantly influence its reactivity and biological activity. Chlorinated compounds are known for their enhanced lipophilicity, affecting how they interact with biological systems.
  • Hydroxyl and Methoxy Groups: The presence of both a hydroxy group and a methoxy group makes this compound particularly interesting. Hydroxy groups are typically involved in hydrogen bonding, while methoxy groups can serve as electron-donating groups, enhancing the compound's overall reactivity.
  • Use in Synthesis: This compound acts as an important intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure has led to explorations in developing novel medicinal compounds that can combat a range of diseases.
  • Natural Occurrence: Derivatives of benzaldehyde can often be found in essential oils and natural flavoring agents. This compound may contribute to the aroma of certain plants, enhancing its appeal in both the cosmetic and food industries.
  • Biological Activity: Studies have indicated that compounds similar to 2,3-dichloro-4-hydroxy-5-methoxy-benzaldehyde exhibit antimicrobial and anti-inflammatory properties, making them a subject of interest for drug development.

As a scientist or a chemistry student, understanding the potential of compounds like 2,3-dichloro-4-hydroxy-5-methoxy-benzaldehyde not only enriches your knowledge base but also opens the door to innovative applications in science and industry. Its complex structure is a testament to the elegance of organic chemistry!

Synonyms
5,6-Dichlorovanillin
18268-69-4
2,3-DICHLORO-4-HYDROXY-5-METHOXYBENZALDEHYDE
Benzaldehyde, 2,3-dichloro-4-hydroxy-5-methoxy-
2,3-dichloro-4-hydroxy-5-methoxy-benzaldehyde
orb1691443
SCHEMBL7966625
DTXSID2075138
LQDPWXPJJUUISU-UHFFFAOYSA-N
AKOS030576734
DB-332758
HY-133607
CS-0128384