CAS 2393-23-9

4-Methoxybenzylamine

Description:

4-Methoxybenzylamine, with the CAS number 2393-23-9, is an organic compound characterized by the presence of a methoxy group (-OCH3) attached to a benzylamine structure. This compound features a benzene ring substituted with a methoxy group at the para position relative to the amine (-NH2) functional group. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. 4-Methoxybenzylamine is known for its role as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It exhibits basic properties due to the amine group, allowing it to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety data indicates that, like many amines, it should be handled with care, as it may cause irritation to the skin and eyes. Proper storage and handling procedures are essential to ensure safety in laboratory and industrial settings.

Formula: C₈H₁₁NO

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

InChI key: InChIKey=IDPURXSQCKYKIJ-UHFFFAOYSA-N

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

Synonyms:

• (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

Formula: C₈H₁₁NO

Purity: >97.0%(GC)(T)

Color and Shape: Colorless to Light yellow to Light orange clear liquid

Molecular weight: 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

Formula: C₈H₁₁NO

Purity: 98+%

Color and Shape: Clear or slightly turbid colorless to pale yellow, Liquid

Molecular weight: 137.18

Ref: 02-A14999

4-Methoxybenzylamine

CAS: 2393-23-9

Formula: C₈H₁₁NO

Purity: 98%

Color and Shape: Liquid

Molecular weight: 137.1790

Ref: IN-DA00343G

4-Methoxybenzylamine

CAS: 2393-23-9

Formula: C₈H₁₁NO

Molecular weight: 137.18

Ref: 7W-GK3141

4-Methoxybenzylamine

CAS: 2393-23-9

4-Methoxybenzylamine

Formula: C₈H₁₁NO

Purity: 98%

Color and Shape: clear. faint yellow liquid

Molecular weight: 137.18g/mol

Ref: 54-OR5028

4-Methoxybenzylamine

CAS: 2393-23-9

Formula: C₈H₁₁NO

Purity: 99.0%

Color and Shape: Liquid

Molecular weight: 137.182

Ref: 10-F008876

4-Methoxybenzenemethanamine

Controlled Product

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);

Formula: C₈H₁₁NO

Color and Shape: Neat

Molecular weight: 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

Formula: C₈H₁₁NO

Purity: Min. 95%

Molecular weight: 137.18 g/mol

Ref: 3D-FM36436