CAS 93-44-7
:2-Naphthalenol, 2-benzoate
Description:
2-Naphthalenol, 2-benzoate, also known as 2-naphthyl benzoate, is an organic compound characterized by the presence of a naphthalene ring substituted with a hydroxyl group and a benzoate moiety. It has a molecular formula that reflects its structure, comprising both aromatic and aliphatic components. This compound typically appears as a white to pale yellow solid and is sparingly soluble in water but more soluble in organic solvents such as ethanol and ether. It exhibits properties typical of phenolic compounds, including potential antioxidant activity and the ability to form hydrogen bonds due to the hydroxyl group. 2-Naphthalenol, 2-benzoate is often used in organic synthesis and may serve as an intermediate in the production of various chemical products. Its applications can extend to the fields of pharmaceuticals, agrochemicals, and materials science. As with many organic compounds, safety precautions should be observed when handling it, as it may pose health risks if ingested or inhaled.
Formula:C17H12O2
InChI:InChI=1S/C17H12O2/c18-17(14-7-2-1-3-8-14)19-16-11-10-13-6-4-5-9-15(13)12-16/h1-12H
InChI key:InChIKey=DWJIJRSTYFPKGD-UHFFFAOYSA-N
SMILES:O(C(=O)C1=CC=CC=C1)C2=CC3=C(C=C2)C=CC=C3
Synonyms:- 2-Benzoyloxynaphthalene
- 2-Naphthalenol benzoate
- 2-Naphthalenol, 2-benzoate
- 2-Naphthol, benzoate
- 2-Naphthol, benzoate (8CI)
- 93-44-7
- Benzonaphthol
- Benzoylnaphthol
- Betabenzon
- NSC 5537
- Naphthalen-2-Yl Benzoate
- Ppc 016
- See more synonyms
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Found 5 products.
2-Naphthyl Benzoate
CAS:Formula:C17H12O2Purity:>98.0%(GC)Color and Shape:White to Light yellow to Light red powder to crystalMolecular weight:248.28Naphthalen-2-yl benzoate
CAS:Purity:95.0%Color and Shape:Solid, White - Slightly pale yellow red powderMolecular weight:248.2810058593752-Naphthyl Benzoate
CAS:<p>2-Naphthyl benzoate is a compound that has been used as a fluorescence probe for the chromatographic determination of cardiac glycosides. It is also an acid conjugate of 2-naphthyl benzoate. The method includes the use of potassium dichromate and other reagents in vitro to determine the presence of cardiac glycosides by measuring fluorescence intensity. The reagents are mixed together, then incubated at 37°C for 5 minutes, followed by addition of the sample. Fluorescence is measured using a spectrophotometer at an excitation wavelength of 340 nm and emission wavelength of 460 nm. A constant that is specific to each cardiac glycoside is used to calculate the amount present in mg/L or µg/mL after 20 minutes. The nucleophilic nature of 2-naphthyl benzoate allows it to react with dipole-dipole interactions with electron deficient heterocyclic rings,</p>Formula:C17H12O2Purity:Min. 95%Color and Shape:PowderMolecular weight:248.28 g/mol




