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Ethylene glycol diformate

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Identification
Molecular formula
C4H6O4
CAS number
3565-36-8
IUPAC name
2-formyloxyethyl formate
State
State

At room temperature, ethylene glycol diformate is a liquid.

Melting point (Celsius)
-35.00
Melting point (Kelvin)
238.15
Boiling point (Celsius)
140.00
Boiling point (Kelvin)
413.15
General information
Molecular weight
118.10g/mol
Molar mass
118.0960g/mol
Density
1.1900g/cm3
Appearence

Ethylene glycol diformate appears as a colorless liquid. It has a faint, pleasant odor and is also known as a diformate ester of ethylene glycol.

Comment on solubility

Solubility of 2-Formyloxyethyl Formate

2-Formyloxyethyl formate, with the chemical formula C5H10O4, exhibits distinct solubility properties that are worth noting:

  • Solvent Compatibility: This compound is generally soluble in polar organic solvents, making it a suitable candidate for a variety of applications in organic synthesis.
  • Water Solubility: Due to the presence of multiple functional groups, its solubility in water is somewhat limited; however, it may dissolve to a minor extent depending on temperature and pH conditions.
  • Temperature Influence: As with many organic compounds, increasing the temperature can enhance solubility, allowing practical applications in heated systems.

In summary, while 2-formyloxyethyl formate is not highly soluble in water, its compatibility with various organic solvents provides versatility in laboratory and industrial settings. Understanding the solubility characteristics of this compound can lead to optimized usage in chemical processes.

Interesting facts

Interesting Facts about 2-formyloxyethyl Formate

2-formyloxyethyl formate is a fascinating compound that has garnered attention in various fields of chemistry and industry due to its unique properties and potential applications. Here are some intriguing aspects of this compound:

Key Features

  • Intermediary Role: This compound serves as an important intermediate in the synthesis of various chemical derivatives, showcasing its versatility in organic synthesis.
  • Solvent Potential: Its structure suggests possible utility as a solvent in chemical reactions, particularly in organic mediums.
  • Biochemical Applications: Research suggests that compounds like 2-formyloxyethyl formate may interact with biological systems, opening avenues for potential pharmaceuticals or agrochemicals.

Reactivity and Stability

Examining the reactivity of 2-formyloxyethyl formate reveals several interesting traits:

  • Nucleophilicity: The presence of the formyloxy group can enhance the compound's nucleophilic character, making it valuable for substitution reactions.
  • Stability Concerns: While generally stable under standard conditions, its reactivity can be influenced by the presence of acids or bases in its environment.

Quote from a Chemist

As one notable chemist remarked, "Understanding the nuanced behaviors of compounds like 2-formyloxyethyl formate not only enriches our knowledge of organic chemistry but also elevates our capacity for innovation in synthetic methodologies."

In conclusion, 2-formyloxyethyl formate may not be the most widely recognized compound, but its roles in chemistry and potential applications make it a subject worth studying further. Whether in academic research or industrial production, its relevance continues to grow.

Synonyms
629-15-2
Ethylene glycol diformate
Ethylene diformate
1,2-Ethanediol, diformate
Glycol diformate
Formic acid, ethylene ester
ETHYLENE GLYCOL, DIFORMATE
1,2-Ethanediol diformate
1,2-Ethanediol, 1,2-diformate
NSC 8831
EINECS 211-077-7
BRN 1746362
AI3-15351
DTXSID4060866
EC 211-077-7
4-02-00-00037 (Beilstein Handbook Reference)
DTXCID9043568
211-077-7
Ethylene formate
1,2-Diformyloxyethane
2-formyloxyethyl formate
1,2-Ethanediol,1,2-diformate
ETHYLENEGLYCOLDIFORMATE
Glycol, diformate
Glykol-diformiat
1, diformate
2-Diformyloxyethane
MFCD00014129
WLN: VHO2OVH
2-(formyloxy)ethyl formate
SCHEMBL827902
CHEMBL2270395
IKCQWKJZLSDDSS-UHFFFAOYSA-
NSC8831
Ethylene glycol diformate, Pract.
1,2-Ethanediol diformate, Pract.
NSC-8831
AKOS006229355
DB-080893
NS00002120
InChI=1/C4H6O4/c5-3-7-1-2-8-4-6/h3-4H,1-2H2