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Glycolic acid allyl ether

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Identification
Molecular formula
C8H12O4
CAS number
61788-61-2
IUPAC name
2-oxoethoxymethyl 2-methylprop-2-enoate
State
State

At room temperature, this compound is in a liquid state.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
206.00
Boiling point (Kelvin)
479.15
General information
Molecular weight
158.18g/mol
Molar mass
158.1700g/mol
Density
1.0557g/cm3
Appearence

The compound is a colorless liquid.

Comment on solubility

Solubility of 2-oxoethoxymethyl 2-methylprop-2-enoate

The solubility of 2-oxoethoxymethyl 2-methylprop-2-enoate (C8H12O4) is influenced by several factors, making it an interesting compound in terms of its behavior in various solvation environments. This compound exhibits moderate solubility in both polar and non-polar solvents, which can be attributed to its molecular structure.

Factors Affecting Solubility

  • Polarity of Solvents: 2-oxoethoxymethyl 2-methylprop-2-enoate is more soluble in polar solvents such as water and alcohols due to its functional groups that can engage in hydrogen bonding.
  • Molecular Size: The relatively low molecular weight allows for better solvation by solvent molecules, enhancing its solubility.
  • Functional Groups: The presence of ester and ketone functional groups in the structure facilitates interactions with various solvents.

As a general rule, compounds that are polar in nature tend to be more soluble in polar solvents, while non-polar compounds prefer non-polar solvents. This particular compound exemplifies the concept of “like dissolves like,” which is a fundamental principle in chemistry. Thus, when considering the solubility of 2-oxoethoxymethyl 2-methylprop-2-enoate, it is important to choose the right solvent for effective dissolution.

Interesting facts

Interesting Facts About 2-oxoethoxymethyl 2-methylprop-2-enoate

2-oxoethoxymethyl 2-methylprop-2-enoate, often referred to as a versatile compound in various chemical applications, holds a fascinating place in the world of organic chemistry. This compound is classified as an ester, which are known for their pleasant aromas and are commonly used in the fragrance industry. Here are some intriguing aspects of this compound:

  • Reactivity: Due to its carbonyl (C=O) group, 2-oxoethoxymethyl 2-methylprop-2-enoate is reactive and can participate in various nucleophilic addition reactions. This makes it an essential precursor in synthetic organic chemistry.
  • Applications: Esters like this compound are widely used in the production of polymers, adhesives, and coatings. They serve as critical intermediates in the synthesis of more complex organic molecules.
  • Biological Significance: Many esters share a natural occurrence, contributing to the aroma of fruits and flowers. They play an essential role in the flavor industry and may be used to create food additives that mimic these natural fragrances.
  • Structural Insights: The unique structure of 2-oxoethoxymethyl 2-methylprop-2-enoate allows for various configurations. Studying its geometry can provide valuable insights into reaction mechanisms and molecular interactions.

As students and scientists delve deeper into the study of 2-oxoethoxymethyl 2-methylprop-2-enoate, they uncover the significant role it plays in both academia and industry. Its utility and reactivity ensure it remains an essential component for many researchers looking to innovate in the field of organic compounds.


Synonyms
METHACRYLIC ACID, CARBOMETHOXYMETHYL ESTER
Carbomethoxymethyl methacrylate
BRN 1771687
AI3-08762
DTXSID00157982
2-Propenoic acid, 2-methyl-, 2-methoxy-2-oxoethyl ester
3-03-00-00380 (Beilstein Handbook Reference)
DTXCID3080473
13318-09-7
2-oxoethoxymethyl 2-methylprop-2-enoate
50G
NRSZKYOGFLBOGH-UHFFFAOYSA-N
2-Oxoethoxymethyl2-methylprop-2-enoate