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2-Methoxynaphthalene, 98%, Thermo Scientific Chemicals
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Catalog number A17650.30
also known as A17650-30
Price (USD)/ Each
42.65
Online exclusive
47.10 Save 4.45 (9%)
-
Quantity:
250 g
Price (USD)/ Each
42.65
Online exclusive
47.10 Save 4.45 (9%)
2-Methoxynaphthalene, 98%, Thermo Scientific Chemicals
Catalog numberA17650.30
Price (USD)/ Each
42.65
Online exclusive
47.10 Save 4.45 (9%)
-
Chemical Identifiers
CAS93-04-9
IUPAC Name2-methoxynaphthalene
Molecular FormulaC11H10O
InChI KeyLUZDYPLAQQGJEA-UHFFFAOYSA-N
SMILESCOC1=CC=C2C=CC=CC2=C1
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Specifications
Specification Sheet
Specification SheetFormCrystals or powder or crystalline powder
Appearance (Color)White to yellow-brown
Melting Point (clear melt)70.0-77.0°C
Assay (GC)≥97.5%
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.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
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.
Solubility
Soluble in benzene, carbon disulfide, diethyl ether. Insoluble in water.
Notes
Keep container tightly closed. Store away from oxidizing agents.
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.
Solubility
Soluble in benzene, carbon disulfide, diethyl ether. Insoluble in water.
Notes
Keep container tightly closed. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- Eric A. Gunnewegh.; Saritha S. Gopie.; Herman van Bekkum. MCM-41 type molecular sieves as catalysts for the Friedel-Crafts acylation of 2-methoxynaphthalene. Journal of Molecular Catalysis A: Chemical. 1996, 106, (1-2), 151-158.
- P. Andy.; J. Garcia-Martinez.; G. Lee.; H. Gonzalez.; C.W. Jones.; M.E. Davis. Acylation of 2-Methoxynaphthalene and Isobutylbenzene over Zeolite Beta. Journal of Catalysis. 2000, 192, (1), 215-223.
- The 3-lithio-derivative (n-BuLi) has been reacted with electrophiles, e.g. allyl bromide, ethylene oxide, etc.: Chem. Ind. (London), 1529 (1963); Indian J. Chem., 7, 536 (1969).
- For Friedel-Crafts acylation at the 6-position, see: Org. Synth. Coll., 6, 34 (1988). For conditions for minimizing the competing 1-acylation, see: Synth. Commun., 20, 383 (1990).