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(2-chloro-2-oxo-ethyl) acetate

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Identification
Molecular formula
C4H5ClO3
CAS number
2631-37-0
IUPAC name
(2-chloro-2-oxo-ethyl) acetate
State
State

It is a liquid at room temperature.

Melting point (Celsius)
-46.70
Melting point (Kelvin)
226.45
Boiling point (Celsius)
136.00
Boiling point (Kelvin)
409.15
General information
Molecular weight
136.54g/mol
Molar mass
136.5410g/mol
Density
1.2435g/cm3
Appearence

The compound appears as a colorless to pale yellow liquid.

Comment on solubility

Solubility of (2-chloro-2-oxo-ethyl) acetate

(2-chloro-2-oxo-ethyl) acetate, known for its interesting chemical properties, exhibits notable solubility characteristics. Here are key points to consider:

  • Solvent Compatibility: This compound is generally soluble in a variety of organic solvents, such as ethanol and acetone.
  • Water Solubility: While (2-chloro-2-oxo-ethyl) acetate is not highly soluble in water, it can dissolve to some extent due to its polar functional groups.
  • Temperature Dependence: The solubility of this compound can increase with temperature, a common trait for many organic compounds.

In practical applications, the solubility of (2-chloro-2-oxo-ethyl) acetate can be advantageous when considering its use in various chemical reactions and formulations. As a rule of thumb, "like dissolves like" applies here, so it is best to use solvents that share similar polarities for optimal solubility.

Understanding the solubility of (2-chloro-2-oxo-ethyl) acetate can greatly enhance its effectiveness in chemical processes and improve the efficiency of product development.

Interesting facts

Interesting Facts About (2-Chloro-2-oxo-ethyl) Acetate

(2-Chloro-2-oxo-ethyl) acetate is a fascinating compound with a variety of interesting attributes that make it noteworthy in the realm of chemistry. Here are some key points to consider:

  • Reactivity: This compound features both a ketone and an ether functional group, which contributes to its unique chemical reactivity. It can participate in various substitution reactions, making it a valuable intermediate in organic synthesis.
  • Versatility: It is used in the synthesis of pharmaceuticals, agrochemicals, and other vital organic compounds. Its structural elements enable it to be a building block for complex molecules.
  • Biological Activity: The chlorine atom in its structure may influence the compound's biological activity, enhancing its potential as a precursor for medicinal compounds.
  • Analytical Use: (2-Chloro-2-oxo-ethyl) acetate can be analyzed through techniques such as NMR and infrared spectroscopy. These methods provide chemists with insight into the compound's structure and functional groups.
  • Research Applications: Ongoing research investigates its properties and applications in different fields, particularly in materials science where its derivatives may demonstrate novel features.

In summary, (2-Chloro-2-oxo-ethyl) acetate serves as more than just a chemical compound; it plays a significant role in organic chemistry and various industrial applications, making it a compound worth studying.

Synonyms
ACETOXYACETYL CHLORIDE
13831-31-7
2-Chloro-2-oxoethyl acetate
2-Acetoxyacetyl chloride
Acetyl chloride, 2-(acetyloxy)-
Acetyl chloride, (acetyloxy)-
Acetylglycoloyl chloride
Z4S19Y2F8S
EINECS 237-542-4
DTXSID20160579
GLYCOLOYL CHLORIDE, ACETATE
DTXCID2083070
237-542-4
Acetoxyacetylchloride
(2-chloro-2-oxoethyl) acetate
MFCD00011535
acetoxyacetic acid chloride
UNII-Z4S19Y2F8S
(Chlorocarbonyl)methyl acetate
acetoxy acetylchloride
Acetoxy acetyl chloride
acetyloxyacetyl chloride
(acetyloxy)acetyl chloride
Chloro-2-oxoethyl acetate
SCHEMBL5288
alpha-acetoxy acetyl chloride
Acetoxyacetyl chloride, 97%
(2-chloro-2-oxo-ethyl)acetate
(2-chloro-2-oxo-ethyl) acetate
ALBB-013561
BCP32585
STR08793
acetic acid chlorocarbonylmethyl ester
acetic acid chlorocarbonyl-methyl ester
AKOS000121009
acetic acid (2-chloro-2-oxoethyl) ester
DB-042424
CS-0017872
NS00024478
(2-chloranyl-2-oxidanylidene-ethyl) ethanoate
EN300-21419
S12356
A807373
Q27294994
F0001-0475
2-Chloro-2-oxoethyl acetate;2-Acetoxyacetyl chloride;Acetoxyacetylchloride