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Climbazole

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Identification
Molecular formula
C15H15Cl2OS
CAS number
38083-17-9
IUPAC name
5-chloro-2-(4-chloro-2-hydroxy-6-methyl-phenyl)sulfanyl-3-methyl-phenol
State
State

At room temperature, climbazole is a solid. It is typically in the form of a powder and is insoluble in water. However, it shows good solubility in organic solvents such as ethanol and methanol.

Melting point (Celsius)
96.00
Melting point (Kelvin)
369.15
Boiling point (Celsius)
450.90
Boiling point (Kelvin)
724.05
General information
Molecular weight
292.25g/mol
Molar mass
292.1840g/mol
Density
1.2830g/cm3
Appearence

Climbazole appears as a white or almost white crystalline powder. It is typically odorless or has a slight characteristic smell. The compound is stable, although it should be stored away from light and moisture to maintain its integrity.

Comment on solubility

Solubility of 5-chloro-2-(4-chloro-2-hydroxy-6-methyl-phenyl)sulfanyl-3-methyl-phenol

The solubility of the compound 5-chloro-2-(4-chloro-2-hydroxy-6-methyl-phenyl)sulfanyl-3-methyl-phenol can be influenced by several factors, considering its complex structure. This compound features multiple functional groups, which can impact its interactions with solvents.

Factors Affecting Solubility:

  • Polarity: The presence of hydroxyl (-OH) and chlorine (-Cl) groups may enhance the compound's polarity, potentially increasing its solubility in polar solvents such as water.
  • Hydrophilic and Hydrophobic Balance: The balance of hydrophilic (water-attracting) and hydrophobic (water-repelling) regions within the molecule plays a crucial role in determining solubility.
  • Temperature: As is common with many organic compounds, solubility may increase with temperature due to enhanced molecular movement.
  • pH Levels: Variations in pH can affect the ionization of the hydroxyl group, thereby influencing solubility in aqueous solutions.

While the specific solubility of this compound in various solvents has not been widely documented, one could surmise that:

  1. It might exhibit better solubility in organic solvents due to its more complex structure.
  2. The presence of ionic or polar solvents could facilitate dissolution, though this needs empirical assessment.

In conclusion, the solubility characteristics of 5-chloro-2-(4-chloro-2-hydroxy-6-methyl-phenyl)sulfanyl-3-methyl-phenol remain a subject for further investigation to understand its behavior in various environments and applications.

Interesting facts

Interesting Facts about 5-chloro-2-(4-chloro-2-hydroxy-6-methyl-phenyl)sulfanyl-3-methyl-phenol

This compound belongs to a class of chemicals known as phenolic compounds, which are characterized by the presence of hydroxyl groups (-OH) attached to aromatic rings. It exhibits unique properties and potential applications in various fields. Here are some fascinating points about this compound:

  • Pharmaceutical Potential: The compound's structural characteristics suggest it could have interesting biological activities. Compounds with similar structures have been studied for their potential anti-inflammatory and antibacterial properties.
  • Sulfanyl Group Impact: The presence of the sulfanyl (thioether) functional group enhances its reactivity and can confer unique properties to the compound, making it a useful building block in synthetic organic chemistry.
  • Chlorine Atoms: The multiple chlorinated substituents in its structure may influence its chemical behavior, including lipid solubility and biological interactions, which are key factors in drug design.
  • Application in Material Science: Given its phenolic nature, this compound may also find applications in the development of advanced materials, such as polymers, due to its ability to participate in cross-linking reactions.
  • Environmental Impact: The study of chlorinated organic compounds has gained significance due to their environmental persistence. Understanding the degradation pathways of such compounds is crucial in environmental chemistry.

In summary, 5-chloro-2-(4-chloro-2-hydroxy-6-methyl-phenyl)sulfanyl-3-methyl-phenol is an intriguing compound with diverse potential applications and implications. "The exploration of such complex molecules could lead to breakthroughs in various scientific domains."

Synonyms
Chlorbisan
Orbisan
Caswell No. 850
2,2'-Thiobis(4-chloro-6-methylphenol)
EINECS 224-582-2
4418-66-0
HSDB 6438
Q9R857FD35
O-Cresol, 6,6'-thiobis(4-chloro-
EPA Pesticide Chemical Code 064208
BRN 3382921
PHENOL, 2,2'-THIOBIS(4-CHLORO-6-METHYL)-
3-06-00-04494 (Beilstein Handbook Reference)
2,2'-Thiobis[4-chloro-6-methylphenol]
O-CRESOL, 6,6'-THIOBIS[4-CHLORO-
Caswell No 850
6,6'Thiobis(4chloroocresol)
oCresol, 6,6'thiobis(4chloro
DTXCID9021768
2,2'Thiobis(4chloro6methylphenol)
Phenol, 2,2'thiobis(4chloro6methyl)
2,2'Dihydroxy3,3'dimethyl5,5'dichlorodiphenyl sulfide
PHENOL, 2,2'-THIOBIS(4-CHLORO-6-METHYL)-[HSDB]
dtxsid1041768
6,6'-Thiobis(4-chloro-o-cresol)
Phenol, 2,2'-thiobis(4-chloro-6-methyl-
UNII-Q9R857FD35
SCHEMBL5933790
2,2'-Dihydroxy-3,3'-dimethyl-5,5'-dichlorodiphenyl sulfide
Q5102918
PHENOL, 2,2'-THIOBIS(4-CHLORO-6-METHYL)- [HSDB]