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Vinyl 2-[(2,2,2-trifluoroacetyl)amino]acetate

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Identification
Molecular formula
C6H6F3NO3
CAS number
.
IUPAC name
vinyl 2-[(2,2,2-trifluoroacetyl)amino]acetate
State
State

This compound is a solid at room temperature.

Melting point (Celsius)
96.00
Melting point (Kelvin)
369.15
Boiling point (Celsius)
225.00
Boiling point (Kelvin)
498.15
General information
Molecular weight
195.09g/mol
Molar mass
195.0860g/mol
Density
1.5678g/cm3
Appearence

The compound is typically observed as a solid, though its exact color and other specific observable traits are not widely documented.

Comment on solubility

Solubility of Vinyl 2-[(2,2,2-trifluoroacetyl)amino]acetate

The solubility of vinyl 2-[(2,2,2-trifluoroacetyl)amino]acetate in various solvents is influenced by its chemical structure and polar characteristics. Here are some key points to consider:

  • Polar Solvents: The presence of the trifluoroacetyl group introduces a significant degree of polarity, suggesting that this compound is likely to dissolve well in polar solvents such as water and methanol.
  • Non-Polar Solvents: In contrast, solubility in non-polar solvents (like hexane) may be limited due to its polar functional groups that prefer interacting with polar environments.
  • Hydrogen Bonding: The amino group may engage in hydrogen bonding, further enhancing its solubility in polar media.
  • Temperature Effects: Solubility can also vary with temperature; typically, higher temperatures may lead to increased solubility for some compounds.

In summary, while vinyl 2-[(2,2,2-trifluoroacetyl)amino]acetate exhibits promising solubility properties in polar solvents, its performance in non-polar environments is likely to be limited. Understanding these solubility characteristics can facilitate effective applications in various chemical processes.

Interesting facts

Interesting Facts about Vinyl 2-[(2,2,2-trifluoroacetyl)amino]acetate

Vinyl 2-[(2,2,2-trifluoroacetyl)amino]acetate is a fascinating compound that belongs to the family of vinyl esters. This compound is remarkable due to several reasons:

  • Structural Diversity: The presence of both vinyl and acetamide functional groups in its structure gives it a unique reactivity and versatility in organic synthesis.
  • Fluorinated Features: The incorporation of trifluoroacetyl groups enhances the compound’s lipophilicity and stability, making it highly interesting for pharmaceutical applications.
  • Applications: This compound can serve as a building block in the synthesis of more complex organic molecules, especially in the fields of drug design and materials science.
  • Reactivity: The vinyl group can participate in various polymerization reactions, potentially leading to the formation of new materials with valuable properties.

Moreover, the trifluoroacetyl moiety is known to impart unique electronic characteristics, which can influence the compound's reactivity towards nucleophiles and electrophiles. As stated by chemists, "The introduction of fluorine atoms can significantly alter the physical and chemical behavior of organic compounds."

This compound exemplifies how small modifications in molecular structure can yield significant alterations in properties and functionalities, making it a point of interest for studies in both theoretical and applied chemistry.

Synonyms
GLYCINE, N-(TRIFLUOROACETYL)-, VINYL ESTER
687-04-7
N-Trifluoroacetylglycine vinyl ester
BRN 2263021
SCHEMBL16685278
DTXSID80218828
vinyl 2-(2,2,2-trifluoroacetamido)acetate