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2,2,3,4,4-Pentachlorobut-3-enoyl chloride

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Identification
Molecular formula
C4HCl6O
CAS number
6088-84-6
IUPAC name
2,2,3,4,4-pentachlorobut-3-enoyl chloride
State
State

It exists as a liquid at room temperature. The compound may emit an acrid odor due to its reactive functional groups.

Melting point (Celsius)
-22.00
Melting point (Kelvin)
251.15
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.15
General information
Molecular weight
230.31g/mol
Molar mass
230.3130g/mol
Density
1.6000g/cm3
Appearence

2,2,3,4,4-Pentachlorobut-3-enoyl chloride is a colorless to pale yellow liquid. It may appear as a clear or slightly hazy solution depending on its purity and storage conditions.

Comment on solubility

Solubility of 2,2,3,4,4-pentachlorobut-3-enoyl chloride

2,2,3,4,4-pentachlorobut-3-enoyl chloride is known for its unique solubility characteristics, largely influenced by its chlorinated structure.

Generally, it exhibits:

  • Solubility in Organic Solvents: This compound is primarily soluble in non-polar organic solvents such as chloroform, carbon tetrachloride, and dichloromethane due to the overall hydrophobic nature imparted by the pentachlorobut-3-enoyl moiety.
  • Poor Solubility in Water: Its solubility in water is very low, making it insoluble in polar solvents. This is characteristic of many chlorinated organic compounds, which struggle to engage in hydrogen bonding or dipole interactions with water molecules.

These properties make 2,2,3,4,4-pentachlorobut-3-enoyl chloride particularly suited for applications in organic synthesis, where it may be utilized in controlled environments to avoid reactions with aqueous solutions.

In summary, understanding the solubility of this compound is crucial for handling and employing it effectively in various chemical processes. Always remember, “like dissolves like” — a rule that holds true in this case!

Interesting facts

Interesting Facts about 2,2,3,4,4-Pentachlorobut-3-enoyl Chloride

2,2,3,4,4-pentachlorobut-3-enoyl chloride is a fascinating compound that belongs to the category of chlorinated organic compounds. Here are some intriguing points about this compound that demonstrate its significance and versatility:

  • Structure and Reactivity: The unique structure of 2,2,3,4,4-pentachlorobut-3-enoyl chloride allows it to participate in various chemical reactions, particularly those involving nucleophiles. Its high reactivity is attributed to the presence of both the acyl chloride and the highly chlorinated alkene functionalities.
  • Environmental Impact: As a chlorinated compound, there is an increased interest in understanding the environmental implications of 2,2,3,4,4-pentachlorobut-3-enoyl chloride. Chlorinated compounds often exhibit persistence in the environment, raising questions about their degradation and potential toxicity.
  • Use in Synthesis: This compound is often utilized in organic synthesis, particularly in the preparation of other chemical substances, including agrochemicals and pharmaceuticals. Its ability to introduce multiple chlorine atoms into substrates makes it a valuable intermediate.
  • Potential Applications: Research is ongoing to explore the potential applications of 2,2,3,4,4-pentachlorobut-3-enoyl chloride in various fields such as materials science and medicinal chemistry. Some studies suggest it may have properties that could be harnessed in the design of new materials.
  • Caution Required: Due to its reactive nature and the presence of chlorine, handling this compound requires strict safety precautions. It is essential to work in a well-ventilated area and use appropriate protective equipment to avoid any adverse health effects.

In summary, 2,2,3,4,4-pentachlorobut-3-enoyl chloride is more than just a chemical entity; it represents a rich area of study in chemistry, providing insights into synthesis, environmental considerations, and potential applications in various industries.

Synonyms
Pentachloro-3-butenoyl chloride
680-52-4
Perchloro-3-butenoic acid chloride
Pentachloro-3-butenoic acid chloride
BRN 1709421
3-BUTENOYL CHLORIDE, 2,2,3,4,4-PENTACHLORO-
PC-3-BAC
3-Butenoyl chloride, 2,2,3,4,4-pentachloro-,
4-02-00-01497 (beilstein handbook reference)
2,2,3,4,4-pentachlorobut-3-enoyl chloride
SCHEMBL11365538
DTXSID10987419