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Allyl mercaptan

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Identification
Molecular formula
C6H10O2S
CAS number
21729-66-0
IUPAC name
2-methylsulfanylethyl prop-2-enoate
State
State

At room temperature, allyl mercaptan is generally in a liquid state.

Melting point (Celsius)
-72.40
Melting point (Kelvin)
200.75
Boiling point (Celsius)
135.30
Boiling point (Kelvin)
408.45
General information
Molecular weight
132.19g/mol
Molar mass
132.1860g/mol
Density
1.0536g/cm3
Appearence

Allyl mercaptan is a colorless to pale yellow liquid with a strong, typical garlic-like odor. It can have a pungent scent that is characteristic of certain thiol compounds.

Comment on solubility

Solubility of 2-methylsulfanylethyl prop-2-enoate

The solubility of 2-methylsulfanylethyl prop-2-enoate can be influenced by various factors including polarity, temperature, and the presence of solvents. This compound, characterized by its functional groups, presents *unique solubility behaviors*.

Key considerations regarding solubility:

  • Polarity: As an ester, 2-methylsulfanylethyl prop-2-enoate exhibits moderate polarity, which affects its solubility in different solvents.
  • Solvent Compatibility: It tends to be more soluble in organic solvents such as alcohols and ethers, while showing lesser solubility in *polar protic solvents* like water.
  • Temperature Effect: Like many organic compounds, the solubility may increase with temperature due to enhanced molecular movement and interaction with solvent molecules.

In summary, understanding the solubility of 2-methylsulfanylethyl prop-2-enoate is crucial for applications in organic synthesis and product formulation. Thus, exploring various solvent systems can yield optimal results in solubility and reactivity.

Interesting facts

Exploring 2-methylsulfanylethyl prop-2-enoate

2-methylsulfanylethyl prop-2-enoate is a fascinating ester that offers intriguing insights into the world of organic chemistry. Known for its unique structure and functional properties, this compound serves various roles across chemical and industrial applications. Here are some interesting facts:

  • Functional Group: As an ester, 2-methylsulfanylethyl prop-2-enoate contains a carbonyl group (C=O) bound to an alkoxy group (derived from an alcohol), which defines its reactivity profile.
  • Chemical Versatility: This compound is known to be a useful intermediate in organic synthesis, particularly for creating more complex molecules. The ability to modify the methylthio group opens pathways for varied functionalization.
  • Role in Polymerization: The prop-2-enoate moiety invites opportunities for polymerization, making this compound relevant in the production of plastics and resins. Its reactivity can lead to the formation of polymers with desirable properties.
  • Biological Applications: Research indicates that compounds like 2-methylsulfanylethyl prop-2-enoate may have potential in pharmaceuticals, especially in the development of bioactive molecules due to the presence of the sulfur atom.
  • Cultural Significance: The methylthio group often relates to various flavors and fragrances, hinting at possible applications in the food or cosmetic industries.

Understanding 2-methylsulfanylethyl prop-2-enoate opens the door to numerous possibilities in both research and industry. As highlighted by chemists, “The beauty of organic chemistry lies in the potential transformations of simple molecules.” With compounds like this one, we continue to explore the immense creativity and utility that organic compounds provide in our everyday lives.

Synonyms
2-(Methylthio)ethyl acrylate
2-Methylthioethyl acrylate
2-Propenoic acid, 2-(methylthio)ethyl ester
G53AIO8V29
Acrylic acid methylthioethyl ester
EINECS 225-420-3
Ethanol, 2-(methylthio)-, acrylate
BRN 2039465
UNII-G53AIO8V29
DTXSID50197494
ACRYLIC ACID, 2-(METHYLTHIO)ETHYL ESTER
DTXCID60119985
2-Propenoic acid, 2-(methylthio)ethyl ester (9CI)
225-420-3
4836-09-3
2-methylsulfanylethyl prop-2-enoate
methylthioethyl acrylate
SCHEMBL2828789
KAGWLGUCGNNPFW-UHFFFAOYSA-N
NS00046268
Q27278762