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Eugenol acetate

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Identification
Molecular formula
C12H14O3
CAS number
93-28-7
IUPAC name
(4-allyl-2-methoxy-phenyl) acetate
State
State

At room temperature, eugenol acetate exists as a liquid.

Melting point (Celsius)
-24.00
Melting point (Kelvin)
249.15
Boiling point (Celsius)
274.00
Boiling point (Kelvin)
547.15
General information
Molecular weight
206.24g/mol
Molar mass
206.2430g/mol
Density
1.0560g/cm3
Appearence

Eugenol acetate appears as a colorless to pale yellow oily liquid. It is known for its pleasant, spicy, clove-like odor.

Comment on solubility

Solubility of (4-allyl-2-methoxy-phenyl) acetate

(4-allyl-2-methoxy-phenyl) acetate, like many organic compounds, exhibits specific solubility characteristics that can influence its applications and usability in various fields. Understanding the solubility properties of this compound is essential for chemists and researchers.

Key Solubility Considerations:

  • Polarity: The presence of both the methoxy group and the acetate moiety contributes to a balance of polar and non-polar characteristics, affecting its ability to dissolve in different solvents.
  • Solvent Compatibility: It is likely to be soluble in organic solvents such as ethanol, acetone, and ether due to its organic nature and functional groups.
  • Temperature Influence: As with many organic compounds, solubility may increase with temperature, allowing for greater dissolution in warmer conditions.

According to the general rule of thumb in chemistry, “like dissolves like.” Therefore, (4-allyl-2-methoxy-phenyl) acetate's solubility will generally be higher in organic solvents compared to polar solvent systems like water. This behavior highlights the necessity of selecting appropriate solvents for extraction and formulation processes involving this compound.

In summary, while detailed experimental data can provide specific solubility metrics for (4-allyl-2-methoxy-phenyl) acetate, its solubility profile is largely influenced by its molecular structure and interactions with potential solvents. Hence, careful consideration of the solvent system is crucial for optimal efficacy in practical applications.

Interesting facts

Interesting Facts about (4-allyl-2-methoxy-phenyl) acetate

(4-allyl-2-methoxy-phenyl) acetate is a fascinating organic compound belonging to the category of phenyl derivatives, with a unique structure that opens up numerous avenues for exploration in both scientific research and industrial applications. Here are some intriguing points to consider:

  • Natural Occurrence: This compound is structurally similar to natural molecules found in essential oils and other plant extracts, which hints at its potential use in the fragrance and flavor industries.
  • Biological Activity: Research has indicated that compounds of this type may exhibit various biological activities, including antimicrobial and antifungal properties. This could make (4-allyl-2-methoxy-phenyl) acetate of interest in pharmaceutical applications.
  • Synthesis Pathways: The synthesis of (4-allyl-2-methoxy-phenyl) acetate can involve various strategies including esterification reactions. Understanding its synthesis can help in developing more sustainable manufacturing techniques.
  • Analytical Techniques: Scientists often utilize various analytical techniques such as Gas Chromatography-Mass Spectrometry (GC-MS) to characterize and study such compounds. These methods reveal crucial information about their structure and potential functions.
  • Potential Uses: Due to its allyl group, this compound may serve as a precursor for numerous other synthetic chains, paving the way for developing new materials such as polymers and agrochemicals.

This compound can serve as an essential piece of a larger puzzle in organic chemistry. Understanding its properties and potential uses not only contributes to academic knowledge but also encourages innovative applications in different sectors.

Final Thoughts

As we continue to investigate (4-allyl-2-methoxy-phenyl) acetate, we recognize that its unique properties and potential applications highlight the endless possibilities within the realm of chemical compounds. As the famous chemist Marie Curie once said, "Nothing in life is to be feared, it is only to be understood." Each compound presents an opportunity to deepen our understanding of chemistry and its impact on our daily lives.

Synonyms
Eugenol acetate
EUGENYL ACETATE
Acetyleugenol
93-28-7
Aceteugenol
4-Allyl-2-methoxyphenyl acetate
Acetyl eugenol
4-Allyl-2-methoxyphenol acetate
1,3,4-Eugenol acetate
Aceto eugenol
Phenol, 2-methoxy-4-(2-propenyl)-, acetate
Phenol, 4-allyl-2-methoxy-, acetate
FEMA No. 2469
1-Acetoxy-2-methoxy-4-allylbenzene
2-Methoxy-4-(2-propenyl)phenyl acetate
NSC 1242
EINECS 202-235-6
2-Methoxy-4-(2-propen-1-yl)phenyl acetate
(2-methoxy-4-prop-2-enylphenyl) acetate
UNII-V9OSB376X8
BRN 1964745
V9OSB376X8
1,4-Eugenol acetate
AI3-01780
NSC-1242
Phenol, 2-methoxy-4-(2-propen-1-yl)-, 1-acetate
CHEMBL108299
DTXSID5052624
CHEBI:34522
3-06-00-05029 (Beilstein Handbook Reference)
Acetic acid 4-allyl-2-methoxy-phenyl ester
Acetat
acetate phenol
acet eugenol
MFCD00026191
4-allyl-2-methoxy-
acetyl eugenol fg 25
2-methoxy-4-(prop-2-en-1-yl)phenyl acetate
bmse010055
Eugenol acetate (Standard)
1-acetate AI3-01780
BRN 1964745 Phenol
BIDD:ER0670
EUGENYL ACETATE [FCC]
SCHEMBL112232
2-methoxy-4-(2-propenyl)-
EUGENOL ACETATE [FHFI]
DTXCID9031197
FEMA 2469
WLN: 1VOR BO1 D2U1
2-Methoxy-4-(prop-2-enyl)phenyl Acetate (Acetyleugenol)
Eugenyl acetate, >=98%, FCC
NSC1242
Acetyleugenol, analytical standard
2-methoxy-4-(2-propen-1-yl)-
HY-W014612R
11EUA7501
BDBM50240728
s9377
3-(4-acetoxy-3-methoxyphenyl)propene
AKOS015837940
Eugenyl acetate, >=98%, FCC, FG
CCG-266622
CS-W015328
FA11965
HY-W014612
CHEMBL108299 V9OSB376X8
AS-56614
1-(3-methoxy-4-acetoxyphenyl)-2-propene
1-Acetoxy-2-methoxy-4-allylbenzene Phenol
acetate NSC 1242 UNII-V9OSB376X8
E0210
NS00012476
Eugenol acetate 1000 microg/mL in Acetonitrile
acetate 2-methoxy-4-(prop-2-en-1-yl)phenyl acetate
Q27116129
Z28076598
CHEBI:34522 SCCDQYPEOIRVGX-UHFFFAOYSA-N (2-methoxy-4-prop-2-enylphenyl)
202-235-6
InChI=1/C12H14O3/c1-4-5-10-6-7-11(15-9(2)13)12(8-10)14-3/h4,6-8H,1,5H2,2-3H