CAS 947-62-6
:2-Methoxy-1-naphthalenecarboxylic acid
Description:
2-Methoxy-1-naphthalenecarboxylic acid, with the CAS number 947-62-6, is an organic compound characterized by its naphthalene structure substituted with a methoxy group and a carboxylic acid functional group. This compound typically appears as a solid at room temperature and is known for its aromatic properties due to the naphthalene ring. The presence of the methoxy group enhances its solubility in organic solvents while the carboxylic acid group contributes to its acidity and potential for hydrogen bonding. It is often utilized in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals. The compound's reactivity can be influenced by the electron-donating nature of the methoxy group, which can affect its electrophilic substitution reactions. Additionally, its physical properties, such as melting point and boiling point, can vary based on purity and environmental conditions. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C12H10O3
InChI:InChI=1S/C12H10O3/c1-15-10-7-6-8-4-2-3-5-9(8)11(10)12(13)14/h2-7H,1H3,(H,13,14)
InChI key:InChIKey=OSTYZAHQVPMQHI-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C2=C(C=CC1OC)C=CC=C2
Synonyms:- 1-Naphthalenecarboxylic acid, 2-methoxy-
- 2-Methoxy-1-naphthoic acid
- 1-Naphthoic acid, 2-methoxy-
- 2-Methoxy-1-naphthalenecarboxylic acid
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Found 5 products.
2-Methoxy-1-naphthoic Acid
CAS:Formula:C12H10O3Purity:>98.0%(GC)(T)Color and Shape:White to Light yellow to Light orange powder to crystalineMolecular weight:202.212-Methoxy-1-naphthoic Acid
CAS:Formula:C12H10O3Purity:95%Color and Shape:SolidMolecular weight:202.20602-Methoxy-1-naphthoic Acid
CAS:<p>2-Methoxy-1-naphthoic Acid is a molecule with two methoxy groups and one naphthalene ring. It has been shown to induce DNA adducts in the human epidermoid carcinoma cells, which may be due to its covalent binding to nucleic acids. The frequency of this compound has been shown to shift when it interacts with murine leukemia cells, which may be due to the formation of intramolecular hydrogen bonds. 2-Methoxy-1-naphthoic Acid also has the ability to form hydrogen bonds with other molecules, such as with the chelate ring of metal ions and other organic compounds. This property can be used for techniques such as nuclear magnetic resonance (NMR) spectroscopy and X-ray crystallography.</p>Formula:C12H10O3Purity:Min. 95%Molecular weight:202.21 g/mol




