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2-Methoxynaphthalene

Short Description:

  • Chemical Name:2-Methoxynaphthalene
  • CAS No.:93-04-9
  • Molecular Formula:C11H10O
  • Molecular Weight:158.2
  • Hs Code.:2909.30
  • European Community (EC) Number:202-213-6
  • NSC Number:4171
  • UNII:VX2T1Z50C4
  • DSSTox Substance ID:DTXSID7044392
  • Nikkaji Number:J4.667A
  • Wikipedia:Β-Naphthol methyl ether
  • Wikidata:Q2240068
  • Metabolomics Workbench ID:45758
  • ChEMBL ID:CHEMBL195857
  • Mol file:93-04-9.mol

Product Detail

Product Tags

2-Methoxynaphthalene 93-04-9

Synonyms:2-methoxynaphthalene

Chemical Property of 2-Methoxynaphthalene

● Appearance/Colour:white powder
● Vapor Pressure:0.000228mmHg at 25°C
● Melting Point:70-73 °C(lit.)
● Refractive Index:1.5440 (estimate)
● Boiling Point:272 °C at 760 mmHg
● PKA:0[at 20 ℃]
● Flash Point:102.3 °C
● PSA9.23000
● Density:1.072 g/cm3
● LogP:2.84840

● Storage Temp.:Store below +30°C.
● Solubility.:H2O: soluble (completely)
● Water Solubility.:INSOLUBLE
● XLogP3:3.5
● Hydrogen Bond Donor Count:0
● Hydrogen Bond Acceptor Count:1
● Rotatable Bond Count:1
● Exact Mass:158.073164938
● Heavy Atom Count:12
● Complexity:144

Safty Information

● Pictogram(s):
● Hazard Codes:
● Safety Statements:22-24/25

Useful

Chemical Classes:Other Classes -> Naphthalenes
Canonical SMILES:COC1=CC2=CC=CC=C2C=C1
Descriptionβ-Naphthyl methyl ether has an intensely sweet, floral odor suggestive of orange blossoms. It is free from naphthol by-odor. It has a sweet, strawberry taste. This may be prepared from potassium β-naphthol and methyl chloride at 300°C; by methylation of β-naphthol with dimethyl sulfate or by direct esterification with methyl alcohol.
Uses:2-Methoxynaphthalene is an Impurity of the non-steroidal anti-inflammatory Naproxen (N377525). 2-methoxynaphthalene acylation is used as a model reaction to study the catalytic benefits of delamination. It was also used to study the alkali-metal-mediated manganation (AMMMn) reactions. 2-methoxynaphthalene acylation was used as a model reaction to study the catalytic benefits of delamination. It was also used to study the alkali-metal-mediated manganation (AMMMn) reactions.

Detailed Introduction

2-Methoxynaphthalene is a chemical compound derived from naphthalene by replacing one hydrogen atom with a methoxy (-OCH3) group at position 2 on the naphthalene ring. Its molecular formula is C11H10O and it has a molecular weight of 158.20 grams per mole.2-Methoxynaphthalene is a solid at room temperature, typically appearing as colorless to pale yellow crystals. It has a melting point of about 48-50°C.This compound is commonly used as a starting material in chemical synthesis and organic reactions. It is also utilized as a fragrance additive in various products, such as perfumes and soaps, due to its pleasant smell.

Application

There are several applications of 2-methoxynaphthalene in various industries. Here are a few examples:
Fragrance and Perfume Industry: 2-Methoxynaphthalene is commonly used as a fragrance ingredient in perfumes, colognes, and other scented products. It provides a sweet, floral aroma and is often used in floral and oriental perfumes.
Flavoring Industry: Due to its pleasant floral odor, 2-methoxynaphthalene is used as a flavoring agent in the food and beverage industry. It can add a floral or fruity note to certain food and drink products.
Pharmaceuticals: 2-Methoxynaphthalene is utilized in pharmaceutical research and development. It can be used as an intermediate or precursor in the synthesis of various pharmaceutical compounds.
Chemical Synthesis: This compound can serve as a starting material or intermediate in the synthesis of other organic compounds. It is utilized in the production of dyes, pigments, agrochemicals, and specialty chemicals.
Research and Development: 2-Methoxynaphthalene is commonly used in laboratory research and development as a solvent or reagent in organic chemistry reactions.
It is important to note that the above applications are just a few examples and there may be other uses of 2-methoxynaphthalene in specific industrial or research settings.


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