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Tetrahydrofuran-2-ylmethyl acetate

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Identification
Molecular formula
C8H14O3
CAS number
4455-13-4
IUPAC name
tetrahydrofuran-2-ylmethyl acetate
State
State

At room temperature, tetrahydrofuran-2-ylmethyl acetate is in a liquid state, making it useful as a solvent in various chemical processes.

Melting point (Celsius)
-65.00
Melting point (Kelvin)
208.15
Boiling point (Celsius)
158.00
Boiling point (Kelvin)
431.15
General information
Molecular weight
158.19g/mol
Molar mass
158.1890g/mol
Density
1.0358g/cm3
Appearence

Tetrahydrofuran-2-ylmethyl acetate is typically a clear, colorless liquid that might have a slight ester-like odor. It is known for its use in organic synthesis and as a solvent.

Comment on solubility

Solubility of Tetrahydrofuran-2-ylmethyl Acetate

Tetrahydrofuran-2-ylmethyl acetate, with its unique chemical structure, exhibits certain solubility characteristics that are noteworthy for various applications. Its solubility is influenced primarily by the presence of its ester functional group and the cyclic ether component of the molecule. Here are a few key points regarding its solubility:

  • Polar Nature: As an ester, tetrahydrofuran-2-ylmethyl acetate tends to have enhanced solubility in polar solvents due to its dipole moments.
  • Solvent Compatibility: It readily dissolves in common organic solvents such as ethanol, acetone, and dimethyl sulfoxide (DMSO), making it versatile for chemical reactions.
  • Water Solubility: Despite its polar nature, its solubility in water is relatively limited due to the hydrophobic thiophene components within its structure.
  • Temperature Effects: Increasing temperature can enhance solubility levels, as is common with many organic compounds.

In summary, the solubility of tetrahydrofuran-2-ylmethyl acetate can be described as moderately soluble in polar organic solvents, while showing limited solubility in water. Understanding these aspects can be crucial for scientists working with this compound in various applications.

Interesting facts

Interesting Facts About Tetrahydrofuran-2-ylmethyl Acetate

Tetrahydrofuran-2-ylmethyl acetate, often abbreviated as THF-2-ylmethyl acetate, is a unique compound noteworthy for its versatile applications in various fields of chemistry and industry. Here are some fascinating insights about this compound:

  • Structure: Tetrahydrofuran is a five-membered ring compound that includes an oxygen atom and is a key building block in organic synthesis. The presence of the acetate group introduces additional reactivity, making it a valuable intermediate.
  • Solvent Properties: THF-2-ylmethyl acetate acts as an excellent solvent for a wide range of polar and non-polar substances, making it a preferred choice in polymer chemistry and extraction processes.
  • Applications in Synthesis: Due to its ability to participate in numerous reactions, it is often utilized in synthesizing complex organic molecules, highlighting its importance in pharmaceutical development and materials science.
  • Stability: This compound exhibits considerable chemical stability under various conditions, which is crucial for maintaining the integrity of reactions during industrial processes.
  • Environmental Impact: As a relatively low-toxicity compound, tetrahydrofuran-2-ylmethyl acetate has garnered attention in green chemistry initiatives. Efforts are underway to explore more eco-friendly synthesis routes and applications.

In addition to its chemical properties, tetrahydrofuran-2-ylmethyl acetate opens up avenues for research into new materials and processes. As noted by many chemists, "The versatility of such compounds often dictates their potential impact in advancing technology and sustainability." With ongoing research, the future of this compound holds exciting possibilities!

Synonyms
TETRAHYDROFURFURYL ACETATE
637-64-9
2-Acetoxymethyloxolane
2-Furanmethanol, tetrahydro-, acetate
2-(Acetoxymethyl)tetrahydrofuran
Tetrahydro-2-furanmethyl acetate
Furfuryl alcohol, tetrahydro-, acetate
Tetrahydro-2-furanmethanol acetate
FEMA No. 3055
I1PIW4REZU
2-Furanmethanol, tetrahydro-, 2-acetate
NSC 4872
EINECS 211-296-8
AI3-21209
NSC-4872
2-(ACETOXYMETHYL)OXOLANE
DTXSID30862335
TETRAHYDROFURFURYL ACETATE, [FHFI]
Furfuryl alcohol, tetrahydro-, acetate (8CI)
2Acetoxymethyloxolane
2(Acetoxymethyl)oxolane
Tetrahydro2furanmethyl acetate
2(Acetoxymethyl)tetrahydrofuran
Tetrahydro2furanmethanol acetate
DTXCID80811116
TETRAHYDROFURFURYL ACETATE,
2Furanmethanol, tetrahydro, acetate
2Furanmethanol, tetrahydro, 2acetate
Furfuryl alcohol, tetrahydro, acetate
TETRAHYDROFURFURYL ACETATE [INCI]
211-296-8
oxolan-2-ylmethyl acetate
(oxolan-2-yl)methyl acetate
Tetrahydro-2-furylmethyl acetate
MFCD00022478
(Tetrahydrofuran-2-yl)methyl acetate
(+/-)-TETRAHYDROFURFURYL ACETATE
TETRAHYDROFURFURYL ACETATE, (+/-)-
UNII-I1PIW4REZU
SCHEMBL118897
CHEMBL2287522
AAQDYYFAFXGBFZ-UHFFFAOYSA-
FEMA 3055
Tetrahydrofurfuryl acetate, 97%
NSC4872
CHEBI:169190
Tetrahydro-2-furanylmethyl acetate
Tetrahydro-2-furanylmethyl acetate #
AKOS005206826
Tetrahydrofurfuryl acetate, >=97%, FG
AS-62668
SY036811
CS-0155423
NS00014151
T0105
F16574
Q27280260
InChI=1/C7H12O3/c1-6(8)10-5-7-3-2-4-9-7/h7H,2-5H2,1H3