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Allyl 2-(2-allyloxy-2-oxoethylthio)acetate

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Identification
Molecular formula
C11H16O4S
CAS number
13551-30-5
IUPAC name
allyl 2-(2-allyloxy-2-oxo-ethyl)sulfanylacetate
State
State

At room temperature, allyl 2-(2-allyloxy-2-oxoethylthio)acetate is in a liquid state. As with most organic compounds, it should be handled with appropriate safety measures, including the use of gloves and goggles to prevent exposure.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
345.00
Boiling point (Kelvin)
618.15
General information
Molecular weight
246.31g/mol
Molar mass
246.3050g/mol
Density
1.0892g/cm3
Appearence

Allyl 2-(2-allyloxy-2-oxoethylthio)acetate appears as a clear to yellowish liquid with a characteristic odor. It is often used in synthesis applications in organic chemistry.

Comment on solubility

Solubility of Allyl 2-(2-allyloxy-2-oxo-ethyl)sulfanylacetate

The solubility of allyl 2-(2-allyloxy-2-oxo-ethyl)sulfanylacetate can be influenced by several factors, such as the presence of functional groups, the molecular structure, and the solvent used. Generally speaking, this compound displays moderate solubility in organic solvents due to the presence of both polar and non-polar components in its structure.

When considering its solubility, it is important to note the following:

  • Polar and Nonpolar Characteristics: The compound contains both polar ether and polar carbonyl functional groups, which can enhance its solubility in polar solvents.
  • Hydrophobic Regions: The allyl groups introduce hydrophobic characteristics, which may limit solubility in highly polar solvents like water.
  • Solvent Compatibility: The solubility is often better in organic solvents such as ethanol, acetone, or dichloromethane, rather than in water.

In summary, the solubility of allyl 2-(2-allyloxy-2-oxo-ethyl)sulfanylacetate can be described as variable depending on the solvent system. Understanding its solubility profile is crucial for various applications in chemistry and material science.

Interesting facts

Interesting Facts about Allyl 2-(2-allyloxy-2-oxo-ethyl)sulfanylacetate

Allyl 2-(2-allyloxy-2-oxo-ethyl)sulfanylacetate is a fascinating compound that showcases the intricate world of organic chemistry. Here are some engaging bits of information about this unique molecule:

  • Versatile Reactivity: This compound participates in a variety of chemical reactions due to the presence of both allyl and sulfonyl functional groups. Its reactivity makes it a potential candidate for organic synthesis.
  • Biological Significance: Compounds with a sulfanyl group have been studied for their biological activities. They may act as enzyme inhibitors or reactants in drug development, highlighting their importance in pharmaceutical chemistry.
  • Applications in Material Science: The unique structure of allyloxy compounds is useful for developing various materials, potentially leading to innovations in polymers and coatings.
  • Unique Functionalization: The presence of the oxo group in the molecule suggests opportunities for further functionalization, enabling chemists to create more complex organic structures, which is a key strategy in drug design.

As you explore the world of organic compounds, remember that each molecule, such as allyl 2-(2-allyloxy-2-oxo-ethyl)sulfanylacetate, holds the promise of new discoveries and applications. As noted by chemists, "Each molecule tells a story," and understanding compounds like this one opens the door to a deeper appreciation of chemistry.

Synonyms
Diallyl thiodiacetate
ACETIC ACID, THIODI-, DIALLYL ESTER
6303-03-3
DP7Z8U5UV4
NSC 42204
NSC-42204
UNII-DP7Z8U5UV4
DTXSID70212315
Dimethylsulfide-alpha,alpha'-dicarboxylic acid diallyl ester
DTXCID70134806
prop-2-enyl 2-(2-oxo-2-prop-2-enoxyethyl)sulfanylacetate
WLN: 1U2OV1S1VO2U1
NSC42204
Dimethylsulfide-.alpha., diallyl ester