W509000
2-Methoxynaphthalene
≥99%
Synonym(s):
Methyl 2-naphthyl ether
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About This Item
Linear Formula:
C10H7OCH3
CAS Number:
Molecular Weight:
158.20
UNSPSC Code:
12164502
Flavis number:
4.074
PubChem Substance ID:
EC Number:
202-213-6
Beilstein/REAXYS Number:
1859408
MDL number:
InChI key
LUZDYPLAQQGJEA-UHFFFAOYSA-N
InChI
1S/C11H10O/c1-12-11-7-6-9-4-2-3-5-10(9)8-11/h2-8H,1H3
SMILES string
COc1ccc2ccccc2c1
biological source
synthetic
grade
Kosher
assay
≥99%
bp
274 °C (lit.)
mp
70-73 °C (lit.)
density
1.064 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
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Features and Benefits
Intensely sweet, floral, mild orange blossom
Other Notes
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Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Mingzhang Gao et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 68(3), 459-465 (2010-01-12)
Carbon-11-labeled piperidine ring of N-[omega-(6-methoxynaphthalen-1-yl)alkyl] derivatives were first designed and synthesized as new selective PET sigma(1) receptor probes. The target tracers were prepared by O-[(11)C]methylation of their corresponding phenolic hydroxyl precursors using [(11)C]CH(3)OTf under basic conditions and isolated by a
R R Price et al.
Journal of microencapsulation, 10(2), 215-222 (1993-04-01)
Many natural products that exhibit biocidal activity have poor solubility in water. In order to explore the prolonged delivery of these compounds from microtubules we have utilized 2-methoxynaphthalene as a model to elucidate release characteristics of hydrophobic compounds entrapped in
G M Whited et al.
Bioorganic & medicinal chemistry, 2(7), 727-734 (1994-07-01)
2-Methoxynaphthalene was subjected to biooxidation by whole cells of six organisms: Pseudomonas putida F39/D containing toluene dioxygenase, Escherichia coli JM109(pDTG601), containing recombinant toluene dioxygenase from Pp F39/D, Pseudomonas sp. NCIB 9816/11, containing naphthalene dioxygenase. E. coli JM109(pDTG141), containing recombinant naphthalene
P Di Gennaro et al.
Biotechnology and bioengineering, 93(3), 511-518 (2005-09-30)
The bioconversion of naphthalene to the 1,2-dihydro-1,2-dihydroxy derivative was performed in good yield using an Escherichia coli recombinant strain carrying Pseudomonas fluorescens N3 dioxygenase. However, the efficiency of such transformation is affected by many process parameters, and their optimization is
H Widén et al.
Food additives and contaminants, 22(7), 681-692 (2005-07-16)
Mineral water and soft drinks with a perceptible off-odour were analysed to identify contaminants originating from previous misuse of the refillable polyethylene terephthalate (PET) bottle. Consumers detected the off-odour after opening the bottle and duly returned it with the remaining
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