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1,3-Dichloro-2-methylpropene

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Identification
Molecular formula
C4H6Cl2
CAS number
563-47-3
IUPAC name
1,3-dichloro-2-methyl-prop-1-ene
State
State

At room temperature, 1,3-Dichloro-2-methylpropene is a liquid. Its volatility contributes to its distinctive odor and handling precautions due to its potentially hazardous nature.

Melting point (Celsius)
-84.00
Melting point (Kelvin)
189.15
Boiling point (Celsius)
108.00
Boiling point (Kelvin)
381.00
General information
Molecular weight
111.00g/mol
Molar mass
111.0010g/mol
Density
1.1187g/cm3
Appearence

1,3-Dichloro-2-methylpropene is a colorless to pale-yellow liquid. It can appear clear and sometimes might have a slight tint due to impurities. It has a sharp, pungent odor, typical of chloroalkenes.

Comment on solubility

Solubility of 1,3-Dichloro-2-methyl-prop-1-ene

1,3-Dichloro-2-methyl-prop-1-ene, with the formula C5H7Cl2, is a chemical compound that exhibits unique solubility characteristics due to its molecular structure and the presence of chlorine atoms.

Solubility Characteristics:

  • Polar Nature: The presence of two chlorine atoms contributes to the polarity of the molecule, which can enhance its solubility in polar solvents.
  • Non-Polar Solvents: Conversely, 1,3-dichloro-2-methyl-prop-1-ene may show reduced solubility in non-polar solvents, reflecting the activity of its carbon skeleton.
  • Water Solubility: This compound is generally considered to have limited solubility in water due to its hydrophobic hydrocarbon structure overshadowing the polar characteristics of the dichloro groups.

Overall, the solubility of 1,3-dichloro-2-methyl-prop-1-ene is influenced by both its functional groups and hydrocarbon backbone. As a solvent or chemical reagent, it is important to recognize how these solubility properties can impact its behavior in various chemical reactions and applications.

Interesting facts

Interesting Facts about 1,3-Dichloro-2-methyl-prop-1-ene

1,3-Dichloro-2-methyl-prop-1-ene is a fascinating organic compound with a variety of applications and properties. Here are some notable points about this compound:

  • Structure & Reactivity: This compound features a unique double bond and contains two chlorine atoms substituting hydrogen atoms, which significantly affects its reactivity. It is classified as an alkene due to the presence of the carbon-carbon double bond, making it generally more reactive than saturated hydrocarbons.
  • Industrial Uses: 1,3-Dichloro-2-methyl-prop-1-ene is often utilized in the production of various chemicals that serve as important intermediates in the creation of pesticides, pharmaceuticals, and other organic compounds. It highlights the important role of chlorinated compounds in synthetic chemistry.
  • Environmental Impact: Chlorinated organic compounds are well-known for their persistence in the environment. They can undergo transformation but may still accumulate in the ecosystem, making their study crucial for understanding environmental chemistry.
  • Toxicology: As a chlorinated compound, it’s essential to study its toxic effects on both human health and wildlife. Proper handling and regulation are critical to mitigate any impacts arising from its toxic nature.
  • Historical Significance: The development of chlorinated hydrocarbons, including this compound, has contributed significantly to advancements in agricultural practices, particularly in pest control. However, it has also led to discussions about sustainability and the trend toward developing safer alternatives.

In summary, 1,3-Dichloro-2-methyl-prop-1-ene serves as an excellent example of how organic compounds play essential roles in both industrial applications and environmental chemistry. The intricate balance between its utility and potential risks makes it a compelling subject of study in the field of chemistry.

Synonyms
1,3-Dichloro-2-methyl-1-propene
3375-22-2
1,3-DICHLORO-2-METHYLPROPENE
ZWZWQSKCVXIXQJ-UHFFFAOYSA-N
DTXSID901304296
1-chloro-2-chloromethyl-1-propene