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1,3,3-trichloro-2-(dichloromethyl)prop-1-ene

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Identification
Molecular formula
C4H5Cl5
CAS number
28079-61-2
IUPAC name
1,3,3-trichloro-2-(dichloromethyl)prop-1-ene
State
State

Liquid at room temperature.

Melting point (Celsius)
-44.00
Melting point (Kelvin)
229.15
Boiling point (Celsius)
179.50
Boiling point (Kelvin)
452.65
General information
Molecular weight
210.89g/mol
Molar mass
210.8910g/mol
Density
1.5540g/cm3
Appearence

1,3,3-Trichloro-2-(dichloromethyl)prop-1-ene is a colorless to pale yellow liquid at room temperature.

Comment on solubility

Solubility of 1,3,3-trichloro-2-(dichloromethyl)prop-1-ene

1,3,3-trichloro-2-(dichloromethyl)prop-1-ene is a halogenated compound, which typically affects its solubility in various solvents. The presence of chlorine atoms within the molecular structure tends to confer certain properties:

  • Polar Nature: The chlorine substituents increase the polarity of the molecule, potentially enhancing its solubility in polar solvents.
  • Solubility in Organic Solvents: This compound is more soluble in organic solvents such as benzene, chloroform, and ether, due to the similar nonpolar character of these solvents compared to the hydrocarbon portion of the molecule.
  • Limited Water Solubility: Due to its halogenated structure, the compound exhibits poor solubility in water. The hydrophobic nature of the carbon chain and the bulky chlorine atoms inhibit interaction with water molecules.

In summary, when considering solubility:

  • Expect good solubility in nonpolar and mildly polar organic solvents.
  • Anticipate low solubility in aqueous solutions.
  • Applications may dictate the choice of solvent for effective use.

The overall solubility characteristics of 1,3,3-trichloro-2-(dichloromethyl)prop-1-ene make it essential to match the solvent choice with the compound's polar and nonpolar interactions.

Interesting facts

Interesting Facts about 1,3,3-Trichloro-2-(dichloromethyl)prop-1-ene

1,3,3-Trichloro-2-(dichloromethyl)prop-1-ene, often referred to in scientific circles as a chlorinated hydrocarbon, has captured the attention of chemists due to its unique structure and applications. This compound holds a significant place in the realm of organic chemistry for several reasons:

  • Industrial Applications: It is primarily used in the production of various agrochemicals, specifically pesticides, contributing to enhanced agricultural productivity.
  • Reactivity: Its reactivity is attributed to the presence of multiple chlorine substituents, making it an interesting target for further chemical modifications and reactions.
  • Environmental Impact: As with many halogenated compounds, it raises concerns regarding environmental persistence and toxicity. Research into its degradation pathways is crucial for assessing its impact on ecosystems.
  • Precursor Chemical: The compound serves as a valuable intermediate in synthesizing other complex organic molecules, demonstrating its versatility in synthetic organic chemistry.
  • Research Significance: Ongoing studies focus on its mechanism of action, which sheds light on the behavior of similarly structured chlorinated compounds in both industrial and biological contexts.

As noted by leading chemists, "The unique properties of chlorinated compounds like 1,3,3-trichloro-2-(dichloromethyl)prop-1-ene reflect the delicate interplay between molecular structure and chemical behavior." Such observations underline the importance of understanding these compounds for both advancement in scientific knowledge and responsible industrial practices.

In conclusion, 1,3,3-trichloro-2-(dichloromethyl)prop-1-ene serves as a fascinating example of how particular chemical structures can lead to specific applications and challenges, driving innovation in chemistry and environmental science.

Synonyms
1,3,3-TRICHLORO-2-(DICHLOROMETHYL)PROPENE
14129-82-9
DTXSID30161658