CAS 2393-23-9

4-Metoxibencilamina

Descripción:

4-Metoxibencilamina, con el número CAS 2393-23-9, es un compuesto orgánico caracterizado por la presencia de un grupo metoxi (-OCH3) unido a una estructura de benzilamina. Este compuesto presenta un anillo bencénico sustituido con un grupo metoxi en la posición para en relación con el grupo funcional amina (-NH2). Típicamente es un líquido o sólido incoloro a amarillo pálido, dependiendo de su pureza y forma. 4-Metoxibencilamina es conocido por su papel como intermediario en la síntesis orgánica, particularmente en la producción de productos farmacéuticos y agroquímicos. Exhibe propiedades básicas debido al grupo amina, lo que le permite participar en varias reacciones químicas, incluidas sustituciones nucleofílicas y reacciones de acoplamiento. Además, puede exhibir actividad biológica, lo que lo hace de interés en la química medicinal. Los datos de seguridad indican que, al igual que muchas aminas, debe manejarse con cuidado, ya que puede causar irritación en la piel y los ojos. Los procedimientos adecuados de almacenamiento y manejo son esenciales para garantizar la seguridad en entornos de laboratorio e industriales.

Fórmula: C₈H₁₁NO

InChI: InChI=1S/C8H11NO/c1-10-8-4-2-7(6-9)3-5-8/h2-5H,6,9H2,1H3

Clave InChI: InChIKey=IDPURXSQCKYKIJ-UHFFFAOYSA-N

SMILES: C(N)C1=CC=C(OC)C=C1

Sinónimos:

• (4-Methoxyphenyl)methanamine
• (p-Methoxyphenyl)methanamine
• 1-(4-Methoxyphenyl)methanamine
• 1-Aminomethyl-4-methoxybenzene
• 4-Methoxybenzenemethanamine
• 4-Methoxybenzylamine
• 4-Methoxyphenylmethylamine
• 4-Methyloxybenzylamine
• Anisylamine
• Benzyl Amine, 4-Methoxy-
• Benzylamine, p-methoxy-
• Nsc 9269
• P-Anisilamina
• Para-methoxybenzylamine
• [[4-(Methyloxy)phenyl]methyl]amine
• p-Anisylamin
• p-Anisylamine
• p-Methoxybenzylamine

4-Methoxybenzylamine

CAS: 2393-23-9

Fórmula: C₈H₁₁NO

Pureza: >97.0%(GC)(T)

Forma y color: Colorless to Light yellow to Light orange clear liquid

Peso molecular: 137.18

Ref: 3B-M0870

4-Methoxybenzylamine, 98+%

CAS: 2393-23-9

4-Methoxybenzylamine is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuff. It is also used fine chemical intemediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documenta

Fórmula: C₈H₁₁NO

Pureza: 98+%

Forma y color: Clear or slightly turbid colorless to pale yellow, Liquid

Peso molecular: 137.18

Ref: 02-A14999

4-Methoxybenzylamine

CAS: 2393-23-9

Fórmula: C₈H₁₁NO

Pureza: 98%

Forma y color: Liquid

Peso molecular: 137.1790

Ref: IN-DA00343G

4-Methoxybenzylamine

CAS: 2393-23-9

Fórmula: C₈H₁₁NO

Peso molecular: 137.18

Ref: 7W-GK3141

4-Methoxybenzylamine

CAS: 2393-23-9

4-Methoxybenzylamine

Fórmula: C₈H₁₁NO

Pureza: 98%

Forma y color: clear. faint yellow liquid

Peso molecular: 137.18g/mol

Ref: 54-OR5028

4-Methoxybenzylamine

CAS: 2393-23-9

Fórmula: C₈H₁₁NO

Pureza: 99.0%

Forma y color: Liquid

Peso molecular: 137.182

Ref: 10-F008876

4-Methoxybenzenemethanamine

Producto controlado

CAS: 2393-23-9

Applications 4-Methoxybenzenemethanamine is used in the synthesis of COX2 inhibitors based on a pyrimidine scaffold. Also used in the preparation of SIRT1 inhibitors. Used in anti-cancer treatments.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Tietz, O. et al.: Org. Biomol. Chem., Eur. J. Med. Chem., 69, 125 (2013);

Fórmula: C₈H₁₁NO

Forma y color: Neat

Peso molecular: 137.18

Ref: TR-M260910

4-Methoxybenzylamine

CAS: 2393-23-9

4-Methoxybenzylamine is an organic amine that has a redox potential of -0.14 V (vs. SHE) and a pK a of 10.5. It is used in the synthesis of trifluoroacetic acid esters, which are used as pharmaceutical intermediates. 4-Methoxybenzylamine has been shown to be effective in alleviating pain in animal models, and its mechanism of action may be due to inhibition of the enzyme cyclooxygenase. The kinetic data for this reaction were obtained by studying the deuterium isotope effect, which is characterized by a low energy barrier and rapid reaction rate. The hydrolysis step is also important for the reaction mechanism, with protocatechuic acid being an intermediate product. Hydrochloric acid is needed for dehydration of the reactants, while an aryl halide can be used instead in some cases. In these reactions, there are many possible reaction

Fórmula: C₈H₁₁NO

Pureza: Min. 95%

Peso molecular: 137.18 g/mol

Ref: 3D-FM36436