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Methyl ethanimidate

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Identification
Molecular formula
C3H7NO
CAS number
583-74-8
IUPAC name
methyl ethanimidate
State
State

Methyl ethanimidate is typically in the liquid state at room temperature, making it suitable for various applications in chemical synthesis.

Melting point (Celsius)
-7.00
Melting point (Kelvin)
266.15
Boiling point (Celsius)
105.00
Boiling point (Kelvin)
378.15
General information
Molecular weight
73.10g/mol
Molar mass
73.0950g/mol
Density
1.0090g/cm3
Appearence

Methyl ethanimidate is a colorless to pale yellow liquid. It has a pungent odor and is typically encountered as a solution for its applications in chemical synthesis and research settings.

Comment on solubility

Solubility of Methyl Ethanimidate

Methyl ethanimidate, a compound with the chemical formula C4H9N2O, exhibits interesting solubility characteristics that are worth exploring. Understanding the solubility of this compound is essential for its potential applications in various fields.

  • Solvent Compatibility: Methyl ethanimidate is generally soluble in polar solvents such as water and alcohols. This is largely attributed to the presence of the imine functional group, which can engage in hydrogen bonding.
  • Temperature Dependency: The solubility may increase with temperature, making it beneficial for reactions that are conducted at elevated temperatures.
  • pH Influence: The solubility could also be affected by the pH of the solution, as the ionization state of the molecule can change, enhancing or hindering dissolution.

As with many organic compounds, the specific conditions, such as temperature and the nature of the solvent, will play a crucial role in determining the solubility of methyl ethanimidate. In conclusion, while it is soluble in several polar solvents, the extent of solubility may be influenced by various external factors.

Interesting facts

Interesting Facts About Methyl Ethanimidate

Methyl ethanimidate is a fascinating compound that plays a significant role in organic synthesis, particularly in the field of pharmaceuticals. This compound is often utilized as an intermediate in the production of various bioactive molecules. Here are some intriguing points about methyl ethanimidate:

  • Synthetic Versatility: Methyl ethanimidate serves as a vital building block in the synthesis of various heterocyclic compounds, which are often found in biologically active pharmaceuticals.
  • Reactivity: The compound exhibits unique reactivity patterns, making it a valuable reagent in coupling reactions and other transformations that are crucial in the synthesis of complex organic molecules.
  • Biological Importance: Compounds derived from methyl ethanimidate have been studied for their potential therapeutic effects, including antibacterial and anti-inflammatory activities.
  • Applications in Research: In laboratory settings, it is frequently used for the development of new chemical methodologies, particularly in the synthesis of amides and related functional groups.
  • Environmental Impact: As with many synthetic compounds, studying the environmental impact and degradation pathways of methyl ethanimidate is essential for developing safer chemical processes in line with green chemistry principles.

Overall, methyl ethanimidate is more than just a simple compound; it represents the intricate connections between chemistry, biology, and environmental science. As chemists continue to explore its properties and applications, it’s exciting to think about the potential new materials and therapies that could emerge from further research!

Synonyms
Methyl acetimidate
14777-29-8
Ethanimidic acid, methyl ester
C1O9DI6F4U
DTXSID701315970
DTXCID301033796
ACETIMIDIC ACID, METHYL ESTER
Methyl acetimidate HCl
methyl ethanimidate
UNII-C1O9DI6F4U
BRN 1736771
2-02-00-00181 (Beilstein Handbook Reference)
SCHEMBL763416
orb1703094
SCHEMBL2467877
SJFKGZZCMREBQH-UHFFFAOYSA-N
ALBB-033133
AKOS009157028
DB-063734
HY-165517
EN300-68780
Q27275068