CAS 2471-70-7
:Ácido 6-metoxi-2-naftoico
Descripción:
Ácido 6-metoxi-2-naftoico es un ácido carboxílico aromático caracterizado por su estructura de naftaleno, que presenta un grupo metoxi (-OCH₃) en la posición 6 y un grupo ácido carboxílico (-COOH) en la posición 2. Este compuesto es típicamente un sólido blanco a blanco sucio y es conocido por su solubilidad moderada en disolventes orgánicos, mientras que es menos soluble en agua. Exhibe propiedades típicas de los ácidos naftoicos, incluyendo aplicaciones potenciales en síntesis orgánica y como intermediario en la producción de colorantes, productos farmacéuticos y agroquímicos. La presencia del grupo metoxi puede influir en su reactividad y polaridad, lo que lo convierte en un bloque de construcción útil en varias reacciones químicas. Además, Ácido 6-metoxi-2-naftoico puede exhibir actividad biológica, lo que puede ser de interés en la química medicinal. Al igual que con muchos compuestos orgánicos, el manejo debe hacerse con cuidado, siguiendo los protocolos de seguridad apropiados para mitigar cualquier riesgo asociado con su uso.
Fórmula: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)
Clave InChI:InChIKey=YZBILXXOZFORFE-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=CC2=C(C=C(OC)C=C2)C=C1
Sinónimos:- 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
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Encontrado 13 productos.
6-Methoxy-2-naphthoic Acid
CAS:Fórmula:C12H10O3Pureza:>97.0%(GC)(T)Forma y color:White to Light yellow to Light orange powder to crystalPeso molecular: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>Fórmula:C12H9O3Pureza:98+%Forma y color:Crystals or powder or crystalline powder, White to pale creamPeso molecular:201.20Naproxen Related Compound A (6-methoxy-2-naphthoic acid)
CAS:Carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides etc, nesoiFórmula:C12H10O3Forma y color:White Off-White PowderPeso molecular:202.062992-Naphthalenecarboxylic acid, 6-methoxy-
CAS:Fórmula:C12H10O3Pureza:97%Forma y color:SolidPeso molecular:202.20606-Methoxy-2-naphthoic acid
CAS:6-Methoxy-2-naphthoic acid (6-Methoxy-2-naphthalenecarboxylic acid) is an modulator of NMDAR.Fórmula:C12H10O3Pureza:99.25%Forma y color:White To Off-White Powder Crystals Crystalline Powder And/Or ChunksPeso molecular:202.21Naproxen EP Impurity O (Naproxen USP Related Compound A)
CAS:Fórmula:C12H10O3Forma y color:Off-White SolidPeso molecular:202.216-Methoxynaphthalene-2-carboxylic Acid (6-Methoxy-2-naphthoic Acid; 2-Carboxy-6-methoxynaphthalene)
CAS:Producto controladoFórmula:C12H10O3Forma y color:NeatPeso molecular:202.216-Methoxy-2-naphthoic acid
CAS:6-Methoxy-2-naphthoic acidFórmula:C12H10O3Pureza:97%Forma y color: pale yellow solidPeso molecular:202.21g/mol6-Methoxy-2-naphthoic Acid
CAS:Producto controlado<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>Fórmula:C12H10O3Forma y color:Off-WhitePeso molecular: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>Fórmula:C12H10O3Pureza:Min. 98 Area-%Forma y color:PowderPeso molecular:202.21 g/mol6-Methoxy-2-naphthoic acid
CAS:Fórmula:C12H10O3Pureza:98%Forma y color:Solid, Chunks or Crystalline PowderPeso molecular:202.209












