CAS 2471-70-7
:6-Methoxy-2-naphthoic acid
Description:
6-Methoxy-2-naphthoic acid is an aromatic carboxylic acid characterized by its naphthalene structure, which features a methoxy group (-OCH₃) at the 6-position and a carboxylic acid group (-COOH) at the 2-position. This compound is typically a white to off-white solid and is known for its moderate solubility in organic solvents, while being less soluble in water. It exhibits properties typical of naphthoic acids, including potential applications in organic synthesis and as an intermediate in the production of dyes, pharmaceuticals, and agrochemicals. The presence of the methoxy group can influence its reactivity and polarity, making it a useful building block in various chemical reactions. Additionally, 6-Methoxy-2-naphthoic acid may exhibit biological activity, which can be of interest in medicinal chemistry. As with many organic compounds, handling should be done with care, following appropriate safety protocols to mitigate any risks associated with its use.
Formula:C12H10O3
InChI:InChI=1S/C12H10O3/c1-15-11-5-4-8-6-10(12(13)14)3-2-9(8)7-11/h2-7H,1H3,(H,13,14)
InChI key:InChIKey=YZBILXXOZFORFE-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=CC2=C(C=C(OC)C=C2)C=C1
Synonyms:- 2-Methoxy-6-naphthalenecarboxylic acid
- 2-Naphthalenecarboxylic acid, 6-methoxy-
- 2-Naphthoic acid, 6-methoxy-
- 6-Methoxy-2-naphthalenecarboxylic acid
- 6-Methoxy-2-naphthalenic acid
- 6-Methoxy-naphthalene-2-carboxylic acid
- 6-Methoxynaphthalen-2-carboxylic acid
- 6-Methoxynaphthalene-2-Carboxylate
- NSC 408786
- 6-Methoxy-2-naphthoic acid
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Found 14 products.
6-Methoxy-2-naphthoic Acid
CAS:Formula:C12H10O3Purity:>97.0%(GC)(T)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:202.216-Methoxy-2-naphthoic acid, 98+%
CAS:<p>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 Sci</p>Formula:C12H9O3Purity:98+%Color and Shape:Crystals or powder or crystalline powder, White to pale creamMolecular weight:201.20Naproxen Related Compound A (6-methoxy-2-naphthoic acid)
CAS:Carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides etc, nesoiFormula:C12H10O3Color and Shape:White Off-White PowderMolecular weight:202.062992-Naphthalenecarboxylic acid, 6-methoxy-
CAS:Formula:C12H10O3Purity:97%Color and Shape:SolidMolecular weight:202.20606-Methoxy-2-naphthoic acid
CAS:<p>6-Methoxy-2-naphthoic acid (6-Methoxy-2-naphthalenecarboxylic acid) is an modulator of NMDAR.</p>Formula:C12H10O3Purity:99.25%Color and Shape:White To Off-White Powder Crystals Crystalline Powder And/Or ChunksMolecular weight:202.216-Methoxy-2-naphthoic acid
CAS:<p>6-Methoxy-2-naphthoic acid</p>Purity:≥98%Molecular weight:202.21g/molNaproxen EP Impurity O (Naproxen USP Related Compound A)
CAS:Formula:C12H10O3Color and Shape:Off-White SolidMolecular weight:202.216-Methoxynaphthalene-2-carboxylic Acid (6-Methoxy-2-naphthoic Acid; 2-Carboxy-6-methoxynaphthalene)
CAS:Controlled ProductFormula:C12H10O3Color and Shape:NeatMolecular weight:202.216-Methoxy-2-naphthoic acid
CAS:<p>6-Methoxy-2-naphthoic acid</p>Formula:C12H10O3Purity:97%Color and Shape: pale yellow solidMolecular weight:202.21g/mol6-Methoxy-2-naphthoic Acid
CAS:Controlled Product<p>Impurity Naproxen USP Related Compound A<br>Applications An impurity of Naproxen (N377525) with bactericidal and fungicidal activity. A metabolite of Nabumetone (N200500). Naproxen USP Related Compound A.<br>References Khorana, M.L. et al.: J. Pharmac. Sci., 56, 993 (1967); Ray, J.E. et al.: J. Chrom. Biomed. Appl., 336, 234 (1984);<br></p>Formula:C12H10O3Color and Shape:Off-WhiteMolecular weight:202.216-Methoxy-2-naphthoic acid
CAS:<p>6-Methoxy-2-naphthoic acid (MN) is a cavity amide that has been shown to have an inhibitory effect on the growth of cancer cells. MN has been found to be more effective in inhibiting β-amyrin than caffeine, which may be due to its increased lipophilicity. It also has a higher affinity for adriamycin and enhances its anticancer effects. MN has been shown to be beneficial in treating diabetic patients, as it can reduce blood glucose levels by stimulating insulin release. The pharmacokinetic properties of MN are similar to those of other cavity amides, with rapid absorption and distribution throughout the body. This compound is metabolized in the liver by CYP2C8, CYP2C9, CYP3A4 and CYP3A5 enzymes. Molecular docking analysis of MN with β-amyrin showed that there was a strong interaction between them due to their complementary shapes and charge distributions</p>Formula:C12H10O3Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:202.21 g/mol6-Methoxy-2-naphthoic acid
CAS:Formula:C12H10O3Purity:98%Color and Shape:Solid, Chunks or Crystalline PowderMolecular weight:202.209













