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1-(3-Methyloxiran-2-yl)ethanone

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Identification
Molecular formula
C5H8O2
CAS number
54782-75-3
IUPAC name
1-(3-methyloxiran-2-yl)ethanone
State
State

At room temperature, this compound exists as a liquid.

Melting point (Celsius)
-63.00
Melting point (Kelvin)
210.15
Boiling point (Celsius)
128.00
Boiling point (Kelvin)
401.15
General information
Molecular weight
100.12g/mol
Molar mass
100.1160g/mol
Density
1.0200g/cm3
Appearence

The compound is a colorless liquid. It is visually clear, suggesting a lack of solid particulates.

Comment on solubility

Solubility of 1-(3-methyloxiran-2-yl)ethanone

1-(3-methyloxiran-2-yl)ethanone, a compound featuring an epoxide functional group, demonstrates interesting solubility characteristics pertinent to its structural configuration. The polarity introduced by the epoxide ring and the carbonyl group renders the compound relatively soluble in various solvents. Here's a clearer breakdown of its solubility behavior:

  • Polar Solvents: It shows good solubility in polar solvents such as water and alcohol due to hydrogen bonding and dipole-dipole interactions.
  • Non-Polar Solvents: While less soluble, 1-(3-methyloxiran-2-yl)ethanone can still dissolve in non-polar solvents, albeit to a lower extent, reflecting its partially hydrophobic nature.
  • Temperature Dependence: Like many organic compounds, its solubility may increase with temperature, favoring dissolution processes.

In summary, the solubility of 1-(3-methyloxiran-2-yl)ethanone is influenced by its structural features, allowing it to interact favorably with both polar and non-polar environments. As with many compounds, understanding these solubility traits is crucial for applications in chemical synthesis and formulation.

Interesting facts

Interesting Facts about 1-(3-Methyloxiran-2-yl)ethanone

1-(3-Methyloxiran-2-yl)ethanone is a fascinating compound that belongs to a class of organic molecules known as epoxides. These compounds are characterized by a three-membered cyclic ether structure, which contributes to their unique reactivity and properties.

Key Characteristics:

  • Epoxide Ring: The presence of the epoxide ring in this compound enhances its reactivity, making it a valuable intermediate in various organic synthesis routes.
  • Precursor to Diverse Products: 1-(3-Methyloxiran-2-yl)ethanone can be transformed into a wide array of chemical products, such as alcohols and acids, through ring-opening reactions.
  • Industrial Applications: Compounds featuring epoxide functionality are utilized in the production of resins, adhesives, and coatings, illustrating the practical importance of 1-(3-methyloxiran-2-yl)ethanone.
  • Biological Relevance: Some epoxides have shown potential biological activities, including antimicrobial and anticancer properties, prompting research into their pharmaceutical applications.

The synthesis of 1-(3-methyloxiran-2-yl)ethanone typically involves the reaction of suitable precursors under specific conditions, highlighting the compound's relevance in both academic and industrial chemistry. As a student of chemistry, one must appreciate the *intricacies* that come with manipulating such versatile molecular structures.

Overall, 1-(3-methyloxiran-2-yl)ethanone offers a glimpse into the *dynamic world of organic chemistry*, where the interplay between structure and function paves the way for innovative discoveries and applications.

Synonyms
17257-79-3
1-(3-methyloxiran-2-yl)ethanone
3,4-epoxy-2-pentanone
2-Pentanone, 3,4-epoxy-
2beta-Acetyl-3alpha-methyloxirane
Ethanone, 1-(3-methyloxiranyl)-
3,4-Epoxy-2-pentanone; 1-(3-methyloxiranyl)-ethanone; 1-(3-Methyloxiranyl)ethanone; 1-Acetyl-2-methyloxirane; 2-Acetyl-3-methyloxirane
1-(3-METHYLOXIRANYL)ETHANONE
SCHEMBL11881829
DTXSID60938173
IAHUKWSQLBRAIN-UHFFFAOYSA-N
1-(3-methyloxiran-2-yl)ethan-1-one
3,4-Anhydro-1,5-dideoxypent-2-ulose
3,4-Anhydro-1,5-dideoxypent-2-ulose #