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3-Chloro-1-phenyl-2-propen-1-one

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Identification
Molecular formula
C9H7ClO
CAS number
20469-36-1
IUPAC name
3-chloro-1-phenyl-prop-2-en-1-one
State
State

The compound exists as a solid at room temperature, characterized by its pale yellow tint and crystalline structure.

Melting point (Celsius)
46.00
Melting point (Kelvin)
319.20
Boiling point (Celsius)
282.50
Boiling point (Kelvin)
555.70
General information
Molecular weight
168.59g/mol
Molar mass
168.5880g/mol
Density
1.2150g/cm3
Appearence

3-Chloro-1-phenyl-2-propen-1-one typically appears as a pale yellow crystalline solid. It is known for its characteristic fragrant odor often associated with aromatic ketones.

Comment on solubility

Solubility of 3-chloro-1-phenyl-prop-2-en-1-one

The solubility of 3-chloro-1-phenyl-prop-2-en-1-one, a compound also known by its IUPAC name, can be quite intriguing to discuss. Its solubility properties are influenced by several factors:

  • Polarity: The presence of the chloro group (–Cl) introduces some polarity to the molecule, potentially affecting how it interacts with various solvents.
  • Solvent Type: 3-chloro-1-phenyl-prop-2-en-1-one is expected to be more soluble in organic solvents, such as ethanol or dimethyl sulfoxide (DMSO), due to its hydrophobic character.
  • Temperature Dependency: Like many organic compounds, its solubility may increase with temperature, making higher temperatures favorable for dissolution.

As a rule of thumb in chemistry, "like dissolves like," so for this compound, one would anticipate that it will be less soluble in polar solvents like water, and more so in non-polar or slightly polar organic solvents.

In conclusion, while specific solubility data may vary, understanding the structure and functional groups of 3-chloro-1-phenyl-prop-2-en-1-one provides a strong basis for predicting its solubility behavior in various environments.

Interesting facts

Interesting Facts about 3-Chloro-1-phenyl-prop-2-en-1-one

3-Chloro-1-phenyl-prop-2-en-1-one, also known as Chalcone, is a fascinating organic compound with numerous applications and properties that make it a subject of interest for chemists and researchers alike. Here are some captivating points about this compound:

  • Versatile Precursor: Chalcones serve as important intermediates in organic synthesis, especially in the creation of flavonoids and other natural products.
  • Biological Activities: Studies suggest that compounds with a chalcone structure possess various biological activities, such as anti-inflammatory, antioxidant, and antibacterial properties.
  • Photochemical Properties: The unsaturated double bonds in chalcones allow them to exhibit interesting photochemical behavior, making them significant in research related to light-activated reactions.
  • Color Producer: Chalcones can act as dyes, contributing to vibrant coloration in various applications, including textiles and biological systems.
  • Cross-Coupling Reactions: The presence of the chloro group makes this compound a suitable participant in cross-coupling reactions, which are key for synthesizing more complex organic molecules.
  • Research Tool: Due to their diverse range of reactions and bioactivities, chalcones are frequently explored in medicinal chemistry and pharmacology, showcasing their relevance in drug design.

Given the notable properties and applications of 3-chloro-1-phenyl-prop-2-en-1-one, it remains a captivating topic in organic chemistry, fueling ongoing research and development in various scientific fields.

Synonyms
3-Chloroacrylophenone
2-Propen-1-one, 3-chloro-1-phenyl-
SCHEMBL9190534