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Methyl 2-naphthylacetate

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Identification
Molecular formula
C13H12O2
CAS number
613-62-7
IUPAC name
methyl 2-(1-naphthyl)acetate
State
State

At room temperature, methyl 2-naphthylacetate is typically a liquid. Due to its relatively low melting point, it remains in the liquid state unless significantly cooled.

Melting point (Celsius)
5.00
Melting point (Kelvin)
278.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
200.25g/mol
Molar mass
200.2480g/mol
Density
1.1350g/cm3
Appearence

Methyl 2-(1-naphthyl)acetate is a colorless to pale yellow liquid with a characteristic pleasant, fruity odor, often used in fragrance compositions. The mixture may display a slight opalescence due to physical impurities or variations in the mixture.

Comment on solubility

Solubility of Methyl 2-(1-naphthyl)acetate

Methyl 2-(1-naphthyl)acetate is a compound whose solubility characteristics offer some intriguing insights into its behavior in various solvents. Here are several key points to consider:

  • Polar vs. Nonpolar Solvents: Methyl 2-(1-naphthyl)acetate tends to be more soluble in nonpolar solvents due to its hydrophobic naphthyl group. This makes it a suitable candidate for organic solvent applications.
  • Solubility Limitations: In aqueous environments, this compound demonstrates limited solubility, as polar solvents typically struggle to dissolve nonpolar substances effectively.
  • Temperature Effects: The solubility of this compound can increase with temperature, highlighting the significance of thermodynamic principles in solubility behavior.

Overall, the solubility profile of methyl 2-(1-naphthyl)acetate reflects its chemical structure, showcasing its affinity for nonpolar environments while exhibiting challenges in polar solvents. As a rule of thumb, "like dissolves like," meaning that the nature of the solvent is crucial when evaluating the solubility of this compound.

Interesting facts

Interesting Facts about Methyl 2-(1-naphthyl)acetate

Methyl 2-(1-naphthyl)acetate, commonly recognized for its role in organic synthesis, is a fascinating compound with several intriguing characteristics.

Key Highlights

  • Biological Significance: This compound has shown promise in various biological applications, particularly in the development of pharmaceuticals. Its structure allows it to interact with biological systems in unique ways, which could lead to the discovery of new drug candidates.
  • Flavor and Fragrance: Methyl 2-(1-naphthyl)acetate is often utilized in the fragrance and flavoring industries due to its sweet and fruity aroma. It is used to enhance the sensory profiles of products like perfumes, cosmetics, and food flavorings.
  • Chemical Reactions: Being an ester, it participates in multiple organic reactions, including hydrolysis and transesterification. These reactions are crucial in synthetic chemistry and serve as foundations for various manufacturing processes.
  • Structural Insights: The compound has a distinctive naphthyl group, which contributes to its unique chemical behavior. Naphthalene derivatives are known for their aromatic properties, which can influence the compound's reactivity and stability.

As we explore the world of organic chemistry, compounds like methyl 2-(1-naphthyl)acetate exemplify the beauty of molecular diversity and its potential applications. As stated by many chemists, “The understanding of one compound can often lead to breakthroughs in science and technology.” Exploring these connections can uncover new roles for such compounds in everyday life.

Synonyms
Methyl 1-naphthaleneacetate
2876-78-0
Methyl 1-naphthylacetate
Hormonit
Kartofin
1-NAPHTHALENEACETIC ACID, METHYL ESTER
M 1 (Growth regulator)
Latka M-1
Methyl alpha-naphthylacetate
Methyl naphthaleneacetic acid
Latka M-1 [Czech]
methyl 1-naphthalenylacetate
Naphthaleneacetic acid methyl ester
Methyl .alpha.-naphthylacetate
Methyl 1-naphthaleneacetic acid
NSC 122030
B2TU4BI7PT
.alpha.-Naphthaleneacetic acid methyl ester
Methylester kyseliny 1-naftyloctove
EINECS 220-720-0
alpha-Naphthylacetic acid methyl ester
BRN 1956293
.alpha.-Naphthylacetic acid methyl ester
DTXSID2042143
AI3-02253
Methylester kyseliny 1-naftyloctove [Czech]
NSC-122030
DTXCID0022143
METHYL .ALPHA.-NAPHTHALENEACETATE
NAPHTHALENEACETIC ACID METHYL ESTER, 1-
METHYL ALPHA-NAPHTHALENEACETATE
alpha-Naphthaleneacetic acid methyl ester
220-720-0
1-Naphthaleneacetic Acid Methyl Ester
methyl 2-(naphthalen-1-yl)acetate
Methyl naphthalene-1-acetate
methyl 2-naphthalen-1-ylacetate
Naphthaleneacetic acid, methyl ester
MFCD00004045
1334-87-8
Methyl naphthaleneacetate
UNII-B2TU4BI7PT
1-Naphthyl acetic acid-methyl ester
Enamine_001683
Methyl1-naphthaleneacetate
methyl naphthalen-1-ylacetate
SCHEMBL709403
WLN: L66J B1VO1
Methyl-1-naphtaleneacetic acid
CHEMBL3182503
YGGXZTQSGNFKPJ-UHFFFAOYSA-
1-Naphthylacetic acid methyl ester
HMS1398M11
Methyl 1-naphthaleneacetate, 96%
alpha-naphthaleneacetic methyl ester
Tox21_300665
NSC122030
STL507839
AKOS000295891
naphthalene-1-acetic acid methyl ester
CCG-353649
CS-W015616
NCGC00248133-01
NCGC00254573-01
AC-28035
DS-10168
SY003589
CAS-2876-78-0
DB-019278
alpha-(1-Naphthyl)-acetic acid methyl ester
N0570
NS00028538
EN300-61311
Q27274285
Z19679503
F0701-0041
Methyl 1-naphthaleneacetate, PESTANAL(R), analytical standard
InChI=1/C13H12O2/c1-15-13(14)9-11-7-4-6-10-5-2-3-8-12(10)11/h2-8H,9H2,1H3