Skip to main content

Allylthiopropionate

ADVERTISEMENT
Identification
Molecular formula
C7H12O2S
CAS number
110-66-7
IUPAC name
2-ethylsulfanylethyl prop-2-enoate
State
State

Allylthiopropionate exists as a liquid at room temperature.

Melting point (Celsius)
-40.00
Melting point (Kelvin)
233.15
Boiling point (Celsius)
194.00
Boiling point (Kelvin)
467.00
General information
Molecular weight
146.21g/mol
Molar mass
146.2140g/mol
Density
1.0234g/cm3
Appearence

Allylthiopropionate is typically a clear liquid under standard conditions.

Comment on solubility

Solubility of 2-ethylsulfanylethyl prop-2-enoate

2-ethylsulfanylethyl prop-2-enoate is a compound that presents unique solubility characteristics. Understanding its solubility is essential for various applications, particularly in organic synthesis and material science.

Key Aspects of Solubility

  • Polarity: The solubility of this compound is influenced by its structural features, notably the ethylsulfanyl group, which can impart some degree of polarity.
  • Solvents: It is generally more soluble in organic solvents such as ethanol, acetone, and ether, but may have limited solubility in water. This is common for many organic compounds with similar functional groups.
  • Temperature Dependence: Like many organic compounds, solubility may increase with temperature, enabling better dissolution in solvent systems during reactions.

In summary, while 2-ethylsulfanylethyl prop-2-enoate exhibits essential solubility in various organic solvents, its interaction with polar solvents like water is less favorable. The overall solubility behavior is crucial for its utility in chemical processes, and understanding these properties can aid in choosing the right conditions for handling this compound effectively.

Interesting facts

Interesting Facts about 2-Ethylsulfanylethyl Prop-2-enoate

2-Ethylsulfanylethyl prop-2-enoate is a fascinating compound that falls within the category of thiol esters, which are known for their unique chemical properties and applications. This compound has garnered attention in various fields due to its structural characteristics and reactivity.

Key Characteristics

  • Versatile Reactivity: As an ester, 2-ethylsulfanylethyl prop-2-enoate is highly reactive, allowing it to participate in various chemical reactions including polymerization, transesterification, and even substitution reactions.
  • Functional Group Potential: The presence of the ethylsulfanyl group adds reactivity and can serve as a nucleophile in multiple organic reactions, providing numerous pathways for synthesis.
  • Applications in Synthesis: This compound may be instrumental in the synthesis of more complex molecules, particularly in organic synthesis and medicinal chemistry, where it could act as a building block for drug development.

Importance in Research

Researchers are particularly interested in compounds like 2-ethylsulfanylethyl prop-2-enoate due to their potential roles in the development of:

  • Pharmaceuticals: Its reactive nature may be exploited for creating new therapeutic agents.
  • Materials Science: The properties of such compounds can contribute to the development of novel materials, potentially with enhanced physical properties.
  • Agricultural Chemicals: Similar esters are often evaluated for their effectiveness as agrochemicals and pesticides.

In summary, 2-ethylsulfanylethyl prop-2-enoate represents a class of compounds with immense potential and versatility, making it a subject of interest for chemists and researchers alike. With ongoing studies, the future could reveal new uses and pathways for this compound, emphasizing the ever-evolving landscape of chemical science.

Synonyms
2-(Ethylthio)ethyl acrylate
ACRYLIC ACID, 2-(ETHYLTHIO)ETHYL ESTER
ML8VQF5GGG
2-Propenoic acid, 2-(ethylthio)ethyl ester
DTXSID20164951
.BETA.-(ETHYLTHIO)ETHYL ACRYLATE
DTXCID0087442
BETA-(ETHYLTHIO)ETHYL ACRYLATE
2-Propenoic acid, 2-(ethylthio)ethyl ester (9CI)
239-262-8
15205-68-2
2-ethylsulfanylethyl prop-2-enoate
Ethylthioethyl acrylate
Acrylic acid ethylthioethyl ester
EINECS 239-262-8
BRN 1927528
UNII-ML8VQF5GGG
beta-ethylthioethyl-acrylate
SCHEMBL4888473
AKOS006280127
NS00024958