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Tetrachloroguaiacol

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Identification
Molecular formula
C8H6Cl4O2
CAS number
56961-77-4
IUPAC name
1,2,3,4-tetrachloro-5,6-dimethoxy-benzene
State
State

At room temperature, Tetrachloroguaiacol is a solid.

Melting point (Celsius)
137.00
Melting point (Kelvin)
410.15
Boiling point (Celsius)
322.00
Boiling point (Kelvin)
595.15
General information
Molecular weight
280.99g/mol
Molar mass
280.9910g/mol
Density
1.6432g/cm3
Appearence

Tetrachloroguaiacol typically presents as a white crystalline solid.

Comment on solubility

Solubility of 1,2,3,4-Tetrachloro-5,6-dimethoxy-benzene

The solubility of 1,2,3,4-tetrachloro-5,6-dimethoxy-benzene (C10H8Cl4O2) is an intriguing subject due to its unique structure and chemical properties. As a synthetic aromatic compound, its solubility characteristics are influenced by both its chlorinated and methoxy substituents. Here are some key points regarding its solubility:

  • In water: This compound is generally insoluble in water due to its hydrophobic nature and the significant presence of chlorine atoms that deter interaction with polar water molecules.
  • In organic solvents: It exhibits much better solubility in organic solvents such as:
    1. Chloroform
    2. Benzene
    3. Toluene
  • Solubility trends: As the number of chlorine substituents increases, the compound's solubility in organic solvents typically increases due to:
    1. Decreased molecular symmetry
    2. Enhanced interactiveness with non-polar and slightly polar solvents

In summary, while 1,2,3,4-tetrachloro-5,6-dimethoxy-benzene shows limited solubility in aqueous environments, it is more compatible with various organic solvents, indicating its potential applications in specific chemical processes and formulations.

Interesting facts

Interesting Facts about 1,2,3,4-Tetrachloro-5,6-dimethoxy-benzene

1,2,3,4-Tetrachloro-5,6-dimethoxy-benzene, often referred to in scientific circles as a complex chlorinated aromatic compound, possesses several fascinating characteristics that make it an intriguing subject of study:

  • Chlorination: The molecular structure includes four chlorine atoms, which significantly influence its chemical reactivity and stability. Chlorination is known to enhance biological activity.
  • Applications in Research: This compound is primarily utilized in fields such as organic synthesis and environmental chemistry. Its unique properties allow chemists to explore various reaction mechanisms and properties of chlorinated compounds.
  • Potential Biological Impact: As a chlorinated aromatic compound, it may exhibit interesting biological activity, making it a point of investigation regarding its effects on living organisms.
  • Dimethoxy Groups: The presence of two methoxy groups in its structure contributes to its solubility in organic solvents and can modulate the compound's electronic properties, impacting its reactivity.
  • Environmental Concerns: Due to its chlorinated nature, this compound raises environmental concerns regarding persistence and potential toxicity in ecosystems, signaling the need for responsible handling and disposal.

As you can see, 1,2,3,4-tetrachloro-5,6-dimethoxy-benzene is not just a compound with a complex name; it embodies a wide range of implications in chemistry, from synthetic utility to environmental impact. Exploring this compound can provide valuable insights into both organic chemistry and the broader implications of chlorinated substances in our environment.

Synonyms
Tetrachloroveratrole
944-61-6
Benzene, 1,2,3,4-tetrachloro-5,6-dimethoxy-
UNII-908Y6Q0O54
3,4,5,6-TETRACHLOROVERATROLE
908Y6Q0O54
DTXSID7073939
VERATROLE, 3,4,5,6-TETRACHLORO-
3,4,5,6-TETRACHLORO-1,2-DIMETHOXYBENZENE
DTXCID9048932
ncyhcgguqgdeqw-uhfffaoysa-n
1,2,3,4-Tetrachloro-5,6-dimethoxybenzene
SCHEMBL9215885
AKOS040758481
DB-335771
HY-133605
CS-0128376
NS00002468
1,2,3,4-Tetrachloro-5,6-dimethoxy-benzene
1,2,3,4-Tetrachloro-5,6-dimethoxybenzene #
Q27271308
Benzene, 1,2,3,4-tetrachloro-5,6-dimethoxy-; Veratrole, 3,4,5,6-tetrachloro- (6CI); 1,2,3,4-Tetrachloro-5,6-dimethoxybenzene; 1,2-Dimethoxytetrachlorobenzene; 3,4,5,6-Tetrachloro-1,2-dimethoxybenzene; 3,4,5,6-Tetrachloroveratrole