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1,3-dichloro-2-(chloromethyl)prop-1-ene

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Identification
Molecular formula
C4H6Cl3
CAS number
14247-63-3
IUPAC name
1,3-dichloro-2-(chloromethyl)prop-1-ene
State
State

At room temperature, 1,3-dichloro-2-(chloromethyl)prop-1-ene is a liquid. It is colorless under ideal conditions but could appear slightly colored if impure.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
136.00
Boiling point (Kelvin)
409.15
General information
Molecular weight
147.45g/mol
Molar mass
147.4470g/mol
Density
1.2350g/cm3
Appearence

1,3-Dichloro-2-(chloromethyl)prop-1-ene typically appears as a colorless liquid, although it may have a slight color due to impurities or environmental exposure. The substance may also emit a distinct chemical odor, characteristic of chlorinated hydrocarbons.

Comment on solubility

Solubility of 1,3-Dichloro-2-(chloromethyl)prop-1-ene

1,3-Dichloro-2-(chloromethyl)prop-1-ene, with the chemical formula C4H6Cl3, exhibits specific solubility characteristics due to the presence of chlorine substituents which enhance its reactivity and polar character. Understanding the solubility of this compound is vital for applications in organic synthesis and industrial processes.

General Solubility Behavior

This compound is known to be:

  • Soluble in organic solvents: 1,3-dichloro-2-(chloromethyl)prop-1-ene shows good solubility in non-polar and slightly polar organic solvents such as:
    • Hexane
    • Toluene
    • Chloroform
  • Low solubility in water: The moderate polarity due to the chlorine atoms contributes to its low solubility in water, making it less favorable for aqueous applications.

Factors Influencing Solubility

Several factors may influence the solubility of this compound:

  • Temperature: Increased temperature generally enhances solubility.
  • Protein binding: In biological systems, the ability of this compound to bind to proteins can affect its effective solubility.
  • Interactions with solvent: Polar protic solvents may show different solubility compared to non-polar solvents due to dipole interactions.

In summary, while 1,3-dichloro-2-(chloromethyl)prop-1-ene is not highly soluble in water, its solubility in various organic solvents makes it a versatile compound in chemical processes. Understanding its solubility properties can lead to more effective applications in synthesis and reaction conditions.

Interesting facts

Interesting Facts About 1,3-Dichloro-2-(chloromethyl)prop-1-ene

1,3-Dichloro-2-(chloromethyl)prop-1-ene, a chemical compound exhibiting intriguing properties, has garnered attention in the fields of organic chemistry and environmental science. Here are some remarkable facts about this compound:

  • Structural Insights: This compound is notable for its unique structure, featuring two chloro substituents at the 1 and 3 positions of the propene backbone. The presence of a chloromethyl group at the 2-position contributes to its reactivity.
  • Reactivity: Due to the presence of multiple chlorine atoms, this compound is classified as a reactive halogenated alkene. Such compounds are often involved in various chemical reactions, including nucleophilic substitution and addition reactions.
  • Applications: 1,3-Dichloro-2-(chloromethyl)prop-1-ene plays a role in several industrial applications, particularly as an intermediate in the synthesis of more complex organic molecules, including pharmaceuticals, agrochemicals, and specialty compounds.
  • Environmental Considerations: As a chlorinated compound, it raises concerns regarding environmental impact and safety. Understanding its behavior in ecosystems is vital for assessing risks associated with its use and disposal.
  • Historical Context: Chlorinated compounds like this one have been used in various applications for decades, with an evolving understanding of their safety, regulation, and environmental impact influencing their usage today.

As a scientist or chemistry student, studying compounds like 1,3-dichloro-2-(chloromethyl)prop-1-ene allows for a deeper understanding of organic chemistry principles and highlights the significant interplay between chemical structure and reactivity. Engaging with such compounds can pave the way for innovative advancements in chemical synthesis and environmental science.

Synonyms
1,3-DICHLORO-2-CHLOROMETHYLPROPENE
13245-65-3
DTXSID60157589
DTXCID0080080
SCHEMBL19987667
HPBWGILCMWDPPJ-UHFFFAOYSA-N
AKOS006383192
1-Propene, 1,3-dichloro-2-chloromethyl
8-Methyl-8-azabicyclo[3.2.1]oct-3-yl (2,4-dichlorophenyl)acetate