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(3-chloro-2-oxo-propyl) benzoate

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Identification
Molecular formula
C10H9ClO3
CAS number
52998-10-8
IUPAC name
(3-chloro-2-oxo-propyl) benzoate
State
State

At room temperature, this compound can exist as a viscous liquid or a low melting solid. It is not highly volatile.

Melting point (Celsius)
45.80
Melting point (Kelvin)
318.95
Boiling point (Celsius)
266.20
Boiling point (Kelvin)
539.35
General information
Molecular weight
198.63g/mol
Molar mass
198.6190g/mol
Density
1.3245g/cm3
Appearence

This compound is typically an oily liquid or low melting solid, depending on the specific isomer and conditions. Its appearance can range from colorless to pale yellow.

Comment on solubility

Solubility of (3-chloro-2-oxo-propyl) benzoate

The solubility of (3-chloro-2-oxo-propyl) benzoate can be influenced by several factors, including its molecular structure and the polarity of the solvent used. Here are some key points to understand its solubility:

  • Polarity: (3-chloro-2-oxo-propyl) benzoate, with its ester functional group, tends to have moderate solubility in polar solvents like water and alcohols, while it is more soluble in organic solvents such as ether and chloroform.
  • Hydrophobic and Hydrophilic Balance: The presence of the benzoate moiety and the alkyl group suggests that it may exhibit a balancing act in solubility; the benzoate group is hydrophilic, whereas the chloro-2-oxo-propyl part leans towards hydrophobic characteristics.
  • Temperature Effect: As with many compounds, increasing the temperature typically enhances solubility; thus, experimenting at different temperatures may yield better solubility results for (3-chloro-2-oxo-propyl) benzoate.

In summary, while (3-chloro-2-oxo-propyl) benzoate is expected to be soluble in various solvents, the degree of solubility will vary depending on the conditions applied.

Interesting facts

Interesting Facts about (3-chloro-2-oxo-propyl) benzoate

(3-chloro-2-oxo-propyl) benzoate is a fascinating compound that falls within the realm of organic chemistry, specifically as an ester formed from benzoic acid. Here are some noteworthy points about this intriguing molecule:

  • Chemical Structure: The compound features a chloro group, a ketone functionality, and a benzoate moiety, creating a unique blend of reactivity and stability within its structure.
  • Synthesis: (3-chloro-2-oxo-propyl) benzoate can be synthesized through esterification reactions, where benzoic acid reacts with a chlorinated derivative of propan-2-one.
  • Reactivity: The presence of the chloro substituent makes this compound an excellent electrophile, which can participate in various nucleophilic substitution reactions.
  • Applications: This compound may serve as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, showcasing the versatile applications of ester compounds in the industry.
  • Biological Significance: Due to the presence of both a ketone and a halogen, there is potential for interesting biological activity, making it a subject of research for medicinal chemistry.

In conclusion, the study of (3-chloro-2-oxo-propyl) benzoate can provide insights into complex organic reactions and the development of new synthetic pathways for various applications in science and technology. Its multifaceted nature showcases the beauty and complexity of organic compounds.

Synonyms
Chlorohydroxyacetone benzoate
BENZOIC ACID, CHLOROACETYLMETHYL ESTER
27933-26-2
1-Benzoyloxy-3-chloropropan-2-one
BRN 2265038
2-Propanone, 1-chloro-3-hydroxy-, benzoate
DTXSID20182216
RefChem:327711
DTXCID30104707
3-chloro-2-oxopropyl benzoate
SCHEMBL3829668
CHEMBL3276486
LRCCOISSUIDSEU-UHFFFAOYSA-N
1-benzoyloxy-3-chloro-2-propanon
1-(benzoyloxy)-3-chloro-2-propanone
DB-373094