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1,4-Dimethoxynaphthalene, 96%, Thermo Scientific Chemicals
化学物質識別子
CAS10075-62-4
IUPAC Name1,4-dimethoxynaphthalene
Molecular FormulaC12H12O2
InChI KeyFWWRTYBQQDXLDD-UHFFFAOYSA-N
SMILESCOC1=C2C=CC=CC2=C(OC)C=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)White to cream
FormCrystals or powder or crystalline powder
Assay (GC)≥95.0%
Melting Point (clear melt)82.0-92.0?C
1,4-Dimethoxynaphthalene may be used as a reference molecule during the synthesis, separation and analysis of derivatized naphthalenes.
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
1,4-Dimethoxynaphthalene may be used as a reference molecule during the synthesis, separation and analysis of derivatized naphthalenes.
Solubility
Soluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
1,4-Dimethoxynaphthalene may be used as a reference molecule during the synthesis, separation and analysis of derivatized naphthalenes.
Solubility
Soluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- E.Peter Kuendig; Vincent Desobry; Dana P.Simmons. Regioselectivity in the addition of carbanions to (1,4-dimethoxynaphthalene)tricarbonylchromium. A new entry into anthracyclinone synthesis. J. Am. Chem. Soc. 1983, 105,(23), 6962-6963.
- James L.Bloomer; Kenneth W.Stagliano; Joseph A.Gazzillo. Preparation of functionalized juglone acetates and juglones via 1,4-dimethoxynaphthalene derivatives: synthesis of anthraquinones related to rhein and aloe-emodin. J. Org. Chem. 1993, 58,(27), 7906-7912.