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S-1,2-Ethanediyl-1,2-ethanediol

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Identification
Molecular formula
C8H14O4S
CAS number
627-83-8
IUPAC name
2-(2-acetoxyethylsulfanyl)ethyl acetate
State
State

At room temperature, this compound is in a liquid state.

Melting point (Celsius)
-70.00
Melting point (Kelvin)
203.15
Boiling point (Celsius)
245.50
Boiling point (Kelvin)
518.65
General information
Molecular weight
220.30g/mol
Molar mass
220.3020g/mol
Density
1.0500g/cm3
Appearence

The compound is generally a colorless to pale yellow liquid. It has a characteristic ester-like odor.

Comment on solubility

Solubility of 2-(2-acetoxyethylsulfanyl)ethyl acetate

The solubility of 2-(2-acetoxyethylsulfanyl)ethyl acetate is an intriguing topic, given the unique structure of the compound. In general, the solubility of organic compounds in various solvents can be influenced by a few key factors:

  • Polarity: The presence of acetate groups in the compound may enhance solubility in polar solvents like water and alcohols, while its hydrocarbon-like structure may favor solubility in non-polar solvents.
  • Hydrogen Bonding: The potential for hydrogen bonding between the --OH groups of the acetate and solvents can play a significant role in determining overall solubility.
  • Intermolecular Forces: The combination of dipole-dipole interactions and London dispersion forces might affect solubility in many organic solvents.

Due to these factors, it is generally observed that:

  1. Solubility in water: Moderate, owing to the polar nature of the acetoxy group.
  2. Solubility in organic solvents: Generally favorable in solvents like ethanol, ether, and dimethyl sulfoxide (DMSO).

These properties make 2-(2-acetoxyethylsulfanyl)ethyl acetate an interesting compound for various applications where solubility in both polar and non-polar mediums may be required.

Interesting facts

Interesting Facts about 2-(2-acetoxyethylsulfanyl)ethyl acetate

2-(2-acetoxyethylsulfanyl)ethyl acetate is a unique compound often explored for its intriguing chemical properties and potential applications. Here are some interesting insights about this compound:

  • Synthetic Pathways: This compound can be synthesized through a variety of organic reactions, emphasizing the versatility of chemistry in creating complex molecules from simpler ones. The incorporation of both an acetoxy and a sulfanyl group showcases the advances in synthetic organic chemistry.
  • Functional Groups: The presence of functional groups such as -OAc (acetoxy) and -S (sulfanyl) contributes to its reactivity. These groups can influence the compound's role in nucleophilic substitutions and other chemical reactions.
  • Potential Applications: Compounds like 2-(2-acetoxyethylsulfanyl)ethyl acetate may find utility in medicinal chemistry. The sulfanyl group can enhance biological activity, making it a candidate for further research in drug development.
  • Flavor and Fragrance: Its ester nature may impart pleasant aromas, potentially allowing for exploration in the fragrance and flavor industry. Esters are commonly known for their fruity odors!
  • Research Interest: The compound has garnered attention in academic research due to its unique structure, which can serve as a building block for more complex molecules in drug discovery and material science.

Overall, the study of 2-(2-acetoxyethylsulfanyl)ethyl acetate not only expands our understanding of organic compounds but also highlights the interconnectedness of chemistry with various fields such as pharmacology and industrial applications.

Synonyms
2,2'-Thiodiethanol diacetate
Acetic acid, thiodiethylene ester
4275-28-9
Ethanol, 2,2'-thiobis-, diacetate
ETHANOL, 2,2'-THIODI-, DIACETATE
Bis(beta-thioethyl acetate)
NSC 5661
EINECS 224-276-9
ONY4E2E6U7
BRN 1777857
AI3-05542
NSC-5661
UNII-ONY4E2E6U7
Bis(.beta.-thioethyl acetate)
DTXSID90195414
4-02-00-00219 (Beilstein Handbook Reference)
2,2'-THIOBISETHANOL DIACETATE
DTXCID00117905
224-276-9
hwlinjpylxlany-uhfffaoysa-n
2,2'-Thiodiethyl diacetate
bis-(2-acetoxy-ethyl) sulfide
WLN: 1VO2S2OV1
Ethanol,2'-thiodi-, diacetate
Ethanol,2'-thiobis-, diacetate
SCHEMBL11652510
NSC5661
NS00031231
2-([2-(Acetyloxy)ethyl]sulfanyl)ethyl acetate #