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1,2-Dichloro-3-(3-iodoprop-2-ynoxy)benzene

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Identification
Molecular formula
C9H5Cl2IO
CAS number
1648796-98-6
IUPAC name
1,2-dichloro-3-(3-iodoprop-2-ynoxy)benzene
State
State

At room temperature, 1,2-dichloro-3-(3-iodoprop-2-ynoxy)benzene is a solid. It is stable under standard conditions.

Melting point (Celsius)
65.00
Melting point (Kelvin)
338.15
Boiling point (Celsius)
291.00
Boiling point (Kelvin)
564.15
General information
Molecular weight
319.93g/mol
Molar mass
319.9330g/mol
Density
1.8150g/cm3
Appearence

1,2-Dichloro-3-(3-iodoprop-2-ynoxy)benzene is typically a crystalline solid compound. The compound can appear as white to off-white crystals or powder.

Comment on solubility

Solubility of 1,2-Dichloro-3-(3-iodoprop-2-ynoxy)benzene

The solubility of 1,2-dichloro-3-(3-iodoprop-2-ynoxy)benzene, a complex organic compound, can be influenced by several factors:

  • Polarity: The presence of chlorine and iodine atoms contributes to its overall polarity, which can affect solubility in different solvents.
  • Solvent Type: This compound is likely to be more soluble in organic solvents such as ethanol, acetone, or dichloromethane compared to water due to its hydrophobic nature.
  • Temperature: As with many organic compounds, increasing temperature can enhance solubility by providing more kinetic energy for solute-solvent interactions.
  • Functional Groups: The presence of the ether functional group (from the prop-2-ynoxy portion) may also enhance the solubility in polar organic solvents.

This multi-functional compound's solubility profile is essential for applications in synthesis and formulation, as it affects both the reactivity and usability of the compound in various chemical processes.

Interesting facts

Interesting Facts about 1,2-Dichloro-3-(3-iodoprop-2-ynoxy)benzene

1,2-Dichloro-3-(3-iodoprop-2-ynoxy)benzene is a fascinating compound that offers a variety of intriguing aspects, particularly in the fields of organic chemistry and material science.

Key Characteristics

  • Versatile Applications: This compound is often used in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows it to interact with biological systems in meaningful ways.
  • Halogenated Compound: Being halogenated, it exhibits distinctive reactivity and biological activity. Compounds with halogen functional groups are known for their enhanced properties in organic reactions.
  • Structural Complexity: The presence of both chloro and iodo substituents contributes to the molecule's complexity, making it a useful subject for studies on chemical reactivity and mechanism elucidation.

Research Significance

This compound has attracted attention in recent years due to its role in the development of new synthetic pathways. As chemistry continuously evolves, compounds like 1,2-dichloro-3-(3-iodoprop-2-ynoxy)benzene become essential for exploring new materials and reactions. Researchers are particularly interested in how the differing electronegativities of chlorine and iodine influence the compound's stability and reactivity.

Key Reactions

  • It can undergo nucleophilic substitution reactions, crucial for forming new chemical bonds.
  • In the presence of strong bases, it can participate in elimination reactions, leading to complex derivatives that may have practical applications.

In summary, 1,2-dichloro-3-(3-iodoprop-2-ynoxy)benzene is not just another compound but a pivotal player in the world of organic chemistry, demonstrating how even subtle changes in molecular structure can lead to significant variations in chemical behavior and application potential.

Synonyms
1,2-dichloro-3-(3-iodoprop-2-ynoxy)benzene
13350-05-5
DTXSID00274800