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Methionine methyl ester

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Identification
Molecular formula
C18H35NO2S
CAS number
2964-48-9
IUPAC name
methyl 2-amino-3-(3,7,11-trimethyldodeca-2,6,10-trienylsulfanyl)propanoate
State
State

At room temperature, Methionine methyl ester is typically a liquid.

Melting point (Celsius)
-17.00
Melting point (Kelvin)
256.15
Boiling point (Celsius)
281.00
Boiling point (Kelvin)
554.15
General information
Molecular weight
317.53g/mol
Molar mass
317.5280g/mol
Density
0.8790g/cm3
Appearence

Methionine methyl ester is a clear, colorless to pale yellow liquid. It may have a slight aromatic odor.

Comment on solubility

Solubility of Methyl 2-amino-3-(3,7,11-trimethyldodeca-2,6,10-trienylsulfanyl)propanoate

Methyl 2-amino-3-(3,7,11-trimethyldodeca-2,6,10-trienylsulfanyl)propanoate, with the chemical formula C18H35NO2S, exhibits unique solubility characteristics. Understanding the solubility of this compound is crucial for its applications in various fields.

Factors Influencing Solubility

The solubility of this compound in different solvents can be influenced by several factors:

  • Polarity: The presence of amino and sulfanyl groups contributes to the overall polarity of the molecule, which may enhance its solubility in polar solvents.
  • Hydrophobicity: The long hydrocarbon chain structure suggests a hydrophobic nature, potentially decreasing solubility in water but improving solubility in organic solvents.
  • Temperature: Increased temperature often increases solubility, particularly for compounds with considerable hydrophobic regions.

Solvent Compatibility

Methyl 2-amino-3-(3,7,11-trimethyldodeca-2,6,10-trienylsulfanyl)propanoate is likely to demonstrate variable solubility in:

  • Water: Likely low solubility due to hydrophobic characteristics.
  • Organic solvents: Higher solubility in solvents such as ethanol, acetone, or chloroform.

In summary, the solubility of this compound can be comprehended through its structure and how its different functional groups interact with the solvent environment. Particularly, it is essential to consider how both hydrophilic and hydrophobic elements balance out in determining the overall solubility in selected media.

Interesting facts

Interesting Facts About Methyl 2-Amino-3-(3,7,11-trimethyldodeca-2,6,10-trienylsulfanyl)propanoate

Methyl 2-amino-3-(3,7,11-trimethyldodeca-2,6,10-trienylsulfanyl)propanoate is an intriguing compound with unique characteristics and potential applications. Here are some fascinating insights:

  • Biological Relevance: This compound features a complex structure that may exhibit biological activities. Its amino group suggests potential effectiveness as a building block in pharmaceuticals, particularly in the synthesis of new medicinal agents.
  • Natural Products: The structure of this compound bears a resemblance to various natural metabolites, potentially linking it to biological pathways in plants or other organisms. Its sulfanyl group may contribute to antioxidant properties.
  • Applications in Chemistry: The sophisticated structure hints at a variety of applications in organic synthesis, particularly in creating derivatives for research into biologically active compounds.
  • Chiral Centers: The presence of chiral centers within the compound could lead to interesting stereochemical properties, enhancing its applications in asymmetric synthesis and chiral catalysts.
  • Potential in Material Science: With ongoing advancements in material science, this compound could be explored for its possible utility in developing advanced materials, including polymers and coatings.

In summary, methyl 2-amino-3-(3,7,11-trimethyldodeca-2,6,10-trienylsulfanyl)propanoate stands out due to its complex structure and potential applications across various scientific fields, making it a compound worth investigating further.

Synonyms
S-Farnesylcysteine alpha-carboxyl methyl ester
2-amino-3-(3,7,11-trimethyl-dodeca-2,6,10-trienylsulfanyl)-propionic Acid Methyl Ester
SIEHZFPZQUNSAS-UHFFFAOYSA-N
methyl 2-amino-3-(3,7,11-trimethyldodeca-2,6,10-trienylsulfanyl)propanoate