CAS 62409-13-6

3-Methoxy-α-methylbenzenemethanamine

Description:

3-Methoxy-α-methylbenzenemethanamine, also known by its CAS number 62409-13-6, is an organic compound characterized by its aromatic structure and the presence of both methoxy and amine functional groups. This compound features a methoxy group (-OCH3) attached to a benzene ring, which is further substituted with an α-methyl group and a methanamine moiety. The presence of the methoxy group can influence the compound's solubility and reactivity, often enhancing its lipophilicity. The amine group contributes to its potential as a base and can participate in hydrogen bonding, affecting its interactions in biological systems. This compound may exhibit pharmacological properties, making it of interest in medicinal chemistry. Its structural features suggest potential applications in the synthesis of more complex molecules or as a precursor in various chemical reactions. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

Formula: C₉H₁₃NO

InChI: InChI=1S/C9H13NO/c1-7(10)8-4-3-5-9(6-8)11-2/h3-7H,10H2,1-2H3

InChI key: InChIKey=CJWGCBRQAHCVHW-UHFFFAOYSA-N

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

Synonyms:

• (±)-α-(m-Methoxyphenyl)ethylamine
• Benzenemethanamine, 3-methoxy-α-methyl-, (±)-
• 3-Methoxy-α-methylbenzenemethanamine
• Benzenemethanamine, 3-methoxy-α-methyl-
• (±)-m-Methoxy-α-methylbenzylamine

1-(3-Methoxyphenyl)ethanamine

CAS: 62409-13-6

Formula: C₉H₁₃NO

Purity: 97%

Color and Shape: Liquid

Molecular weight: 151.2056

Ref: IN-DA003CXE

1-(3-Methoxyphenyl)ethanamine

CAS: 62409-13-6

1-(3-Methoxyphenyl)ethanamine

Purity: 98%

Molecular weight: 151.21g/mol

Ref: 54-OR1001123

1-(3-Methoxy-phenyl)-ethylamine

CAS: 62409-13-6

Formula: C₉H₁₃NO

Purity: 97%

Color and Shape: Liquid

Molecular weight: 151.209

Ref: 10-F030159

1-(3-Methoxyphenyl)ethylamine

CAS: 62409-13-6

1-(3-Methoxyphenyl)ethylamine is an enantiomer of the amino acid phenylalanine, and it has been used in the synthesis of racemic drugs. The optical properties of 1-(3-methoxyphenyl)ethylamine are different from those of other amino acids and can be used to create a chiral environment. This molecule can also be used as a calcimimetic that stimulates bone formation by increasing osteoblasts. It also inhibits aminotransferases and increases the production of malic acid, which is important for the synthesis of lactic acid. In addition, this molecule can be used as an efficient method for asymmetric synthesis with organic solvents such as amines or crystallography.

Formula: C₉H₁₃NO

Purity: Min. 95%

Molecular weight: 151.21 g/mol

Ref: 3D-MCA40913