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2,4,5-Trichlorobenzenethiol

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Identification
Molecular formula
C6H3Cl3SH
CAS number
635-45-4
IUPAC name
2,4,5-trichlorobenzenethiol
State
State

At room temperature, 2,4,5-Trichlorobenzenethiol is typically a solid.

Melting point (Celsius)
56.00
Melting point (Kelvin)
329.15
Boiling point (Celsius)
317.00
Boiling point (Kelvin)
590.15
General information
Molecular weight
211.51g/mol
Molar mass
211.5100g/mol
Density
1.5170g/cm3
Appearence

2,4,5-Trichlorobenzenethiol typically appears as a pale yellow solid with a characteristic odor.

Comment on solubility

Solubility of 2,4,5-Trichlorobenzenethiol

2,4,5-trichlorobenzenethiol, a compound with notable structure, displays unique solubility characteristics that reflect its chemical nature. Its solubility can be influenced by various factors, making it an interesting subject of study. Here are some key points regarding its solubility:

  • Solvent Polarity: This compound is expected to be more soluble in polar solvents due to the presence of the thiol (-SH) group which can engage in hydrogen bonding.
  • Chlorine Substituents: The presence of three chlorine atoms enhances the compound's lipophilicity, potentially rendering it less soluble in water but more soluble in organic solvents.
  • Concentration and Temperature: Like many organic compounds, solubility can vary with temperature; higher temperatures typically increase solubility in most solvents.

In summary, the solubility of 2,4,5-trichlorobenzenethiol is multifaceted, influenced by its chemical structure and the solvents involved. Understanding these interactions is crucial for applications in various chemical processes.

Interesting facts

Interesting Facts about 2,4,5-Trichlorobenzenethiol

2,4,5-Trichlorobenzenethiol is a fascinating compound that attracts attention due to its unique structure and applications. Here are some intriguing aspects that highlight its significance in the field of chemistry:

  • Chemical Structure: This compound belongs to the class of chlorobenzenes, characterized by the presence of three chlorine atoms replaced in the benzene ring. The positioning of these atoms at the 2, 4, and 5 positions creates a highly polar structure, leading to distinctive reactivity.
  • Industrial Relevance: 2,4,5-Trichlorobenzenethiol is often used as a reagent in various chemical syntheses, showcasing its importance in manufacturing and industrial processes.
  • Biochemical Significance: Compounds like this one are studied for their potential effects in biological systems, particularly in assessing the impact of chlorinated compounds on ecological and human health.
  • Environmental Considerations: Given its chlorinated nature, researchers are very interested in understanding the environmental fate and bioaccumulation of this compound, which is crucial for risk assessment and management.
  • Toxicity and Safety: While it may have useful applications, 2,4,5-trichlorobenzenethiol also poses certain hazards, making it essential to handle it with care in laboratory settings.

As chemists continue to explore the properties and applications of 2,4,5-trichlorobenzenethiol, they contribute valuable insights into both its utility and its risks. The balance between its functionality and safety is a key consideration for future research and industrial use.

Synonyms
2,4,5-Trichlorothiophenol
3773-14-6
2,4,5-TRICHLOROBENZENETHIOL
Renacit II
Benzenethiol, 2,4,5-trichloro-
EINECS 223-223-7
NSC 41933
BRN 0509727
DTXSID80191167
DTXCID90113658
223-223-7
4-06-00-01635 (beilstein handbook reference)
jarialsgfxecch-uhfffaoysa-n
2,4,5-trichlorobenzene-1-thiol
C6H3Cl3S
MFCD00014447
2,4,5-trichloro-thiophenol
SCHEMBL1436824
2,4,5-Trichlorophenyl Mercaptan
2,4,5-tris(chloranyl)benzenethiol
NSC41933
NSC-41933
AKOS024319187
AS-58528
DB-019806
CS-0267891
NS00030281
T0728
1-Butyl-3-(4-sulfobutyl)imidazolium triflate
D92383
EN300-673725
A843742