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2-Methoxynaphthalene

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Identification
Molecular formula
C11H10O
CAS number
93-04-9
IUPAC name
2-methoxynaphthalene
State
State
2-Methoxynaphthalene is typically a solid at room temperature. It is stable under normal conditions and has notable aromatic properties, being used in perfumery and as an intermediate in various chemical syntheses.
Melting point (Celsius)
73.00
Melting point (Kelvin)
346.00
Boiling point (Celsius)
274.40
Boiling point (Kelvin)
547.50
General information
Molecular weight
158.20g/mol
Molar mass
158.2020g/mol
Density
1.0855g/cm3
Appearence

2-Methoxynaphthalene appears as a light yellow solid. It is often crystalline in nature, presenting with a distinct aromatic odor. The crystals can vary in size and may have a slightly greasy texture when handled.

Comment on solubility

Solubility of 2-methoxynaphthalene

2-methoxynaphthalene, with the chemical formula C11H12O, exhibits interesting solubility characteristics that are worth exploring.

General Solubility

This compound is generally insoluble in water due to its hydrophobic naphthalene structure. However, it demonstrates varied solubility in organic solvents:

  • Soluble in: Organic solvents such as ethanol, ether, and benzene.
  • Insoluble in: Water and polar solvents.

Factors Influencing Solubility

The solubility behavior of 2-methoxynaphthalene can be influenced by:

  • Temperature: Higher temperatures typically increase solubility in organic solvents.
  • Nature of the solvent: Nonpolar solvents enhance solubility due to similar interactions.

Conclusion

In summary, while 2-methoxynaphthalene is insoluble in water, it is soluble in a range of organic solvents, making it a useful compound in various organic synthesis applications. This behavior highlights the importance of understanding solvent interactions in chemical processes.

Interesting facts

Interesting Facts about 2-Methoxynaphthalene

2-Methoxynaphthalene, also known as β-methoxynaphthalene, is an aromatic compound with fascinating properties and applications that capture the interest of chemists and industry professionals alike.

Key Characteristics

  • Aromaticity: This compound is derived from naphthalene, making it a part of a class of compounds that are known for their stability and unique electronic properties due to resonating structures.
  • Substituent Effects: The methoxy group (-OCH3) in this compound plays a significant role in determining reactivity and how the molecule interacts with other substances.
  • Applications: It is often utilized in the production of dyes, fragrances, and as a solvent, which highlights its importance in the chemical industry.

Biological Significance

Interestingly, compounds like 2-methoxynaphthalene can exhibit biological activity:

  • Some studies suggest potential antioxidant properties.
  • It may also possess significant roles in the synthesis of other biologically active substances.

Research and Innovations

The exploration of 2-methoxynaphthalene extends to:

  • Its use in organic synthesis as a building block for more complex chemical structures.
  • Investigations into its environmental impact and degradation pathways, highlighting the importance of sustainable chemistry.

In summary, 2-methoxynaphthalene stands as a remarkable compound, not only for its practical applications in various industries but also for its intriguing chemical behavior and biological interactions. As we delve deeper into the world of organic compounds, uncovering the diverse roles of such substances becomes pivotal for innovation in chemistry.

Synonyms
2-METHOXYNAPHTHALENE
93-04-9
Naphthalene, 2-methoxy-
Nerolin
Yara yara
Methyl 2-naphthyl ether
Yura yara
Yara-Yara
2-Naphthol methyl ether
2-Naphthyl methyl ether
beta-Methoxynaphthalene
Nerolin (old)
beta-Naphthyl methyl ether
2-Methoxy-naphthalene
.beta.-Methoxynaphthalene
beta-Naphthol mether ether
beta-Naphthol methyl ether
Methyl beta-naphthyl ether
2-methoxy naphthalene
Nerolin Yara Yara
NSC 4171
.beta.-Naphthol methyl ether
.beta.-Naphthyl methyl ether
2-Methoxynaphthalene-1-D
2-Methoxynaphthalene-6-D
EINECS 202-213-6
UNII-VX2T1Z50C4
Methyl .beta.-naphthyl ether
VX2T1Z50C4
DTXSID7044392
AI3-21213
NSC-4171
MFCD00004061
2-Methoxynaphthalene(Nerolin)
CHEMBL195857
DTXCID5024392
FEMA NO. 4704
2-METHOXYNAPHTHALENE [MI]
EC 202-213-6
NAPROXEN IMPURITY M [EP IMPURITY]
NAPROXEN SODIUM IMPURITY M [EP IMPURITY]
68251-83-2
68251-84-3
2-NAPHTHOL METHYL ETHER;2-NAPHTHYL METHYL ETHER
NAPROXEN IMPURITY M (EP IMPURITY)
NAPROXEN SODIUM IMPURITY M (EP IMPURITY)
YaraYara
Jara jara
2-Methoxynaphthalene(Nerolin); Naproxen Imp. M (EP); Naproxen Impurity M
2-methoxynaphtalene
2-methoxynapthalene
Nerolin, yara yara
6-methoxynaphthalene
betaMethoxynaphthalene
Naphthalene, 2methoxy
2Naphthol methyl ether
2Naphthyl methyl ether
Methyl 2naphthyl ether
b-naphthyl methyl ether
beta -Methoxynaphthalene
betaNaphthol methyl ether
betaNaphthyl methyl ether
Methyl betanaphthyl ether
beta -Naphthol methyl ether
beta -Naphthyl methyl ether
Methyl beta -naphthyl ether
2-Methoxynaphthalene, 99%
SCHEMBL112792
Nerolin Yara Yara, >=99%
2-Methoxynaphthalene, >=99%
METHYL ?-NAPHTHYL ETHER
SCHEMBL10250691
NSC4171
CHEBI:177835
Tox21_302143
BDBM50159258
MFCD31699956
MFCD31699957
AKOS008947868
AC-4741
CS-W010895
DS-4954
FM25311
HY-W010179
CAS-93-04-9
NCGC00255953-01
PD055399
SY246288
SY246289
DB-014139
M0117
NS00001155
|A-Naphthyl methyl ether 2-Methoxynaphthalene
EN300-58910
D71164
AF-676/00077048
Q2240068
2-Methoxynaphthalene, pharmaceutical impurity standard
Z53835290
2-Naphthol methyl ether;2-Naphthyl methyl ether;6-Methoxy-2-naphthalene