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Atomfair p-methoxy-N-methylphenethylamine Compound 48-80 C10H15NO

Description p-Methoxy-N-methylphenethylamine (CAS No. 4091-50-3) is a high-purity organic compound with the molecular formula C10H15NO. Also known as 2-(4-methoxyphenyl)-N-methylethanamine , this compound is a derivative of phenethylamine featuring a methoxy group at the para position and a methyl substitution on the amine. It is widely utilized in pharmacological and neuroscience research due to its structural similarity to bioactive amines. Our product is synthesized under strict quality control, ensuring ??98% purity (HPLC) and is supplied as a crystalline solid or in solution, depending on researcher requirements. Ideal for use as a reference standard, biochemical reagent, or intermediate in organic synthesis.

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Description

Description

p-Methoxy-N-methylphenethylamine (CAS No. 4091-50-3) is a high-purity organic compound with the molecular formula C10H15NO. Also known as 2-(4-methoxyphenyl)-N-methylethanamine, this compound is a derivative of phenethylamine featuring a methoxy group at the para position and a methyl substitution on the amine. It is widely utilized in pharmacological and neuroscience research due to its structural similarity to bioactive amines. Our product is synthesized under strict quality control, ensuring ??98% purity (HPLC) and is supplied as a crystalline solid or in solution, depending on researcher requirements. Ideal for use as a reference standard, biochemical reagent, or intermediate in organic synthesis.

  • CAS No: 4091-50-3
  • Molecular Formula: C10H15NO
  • Molecular Weight: 165.23
  • Exact Mass: 165.115364102
  • Monoisotopic Mass: 165.115364102
  • IUPAC Name: 2-(4-methoxyphenyl)-N-methylethanamine
  • SMILES: CNCCC1=CC=C(C=C1)OC
  • Synonyms: 4091-50-3, Compound 48-80, p-Methoxy-N-methylphenethylamine, Benzeneethanamine, 4-methoxy-N-methyl-, N-(p-Methoxyphenethyl)methylamine

Application

p-Methoxy-N-methylphenethylamine is primarily used in research settings as a model compound for studying neurotransmitter analogs and receptor interactions. It serves as a precursor in the synthesis of more complex pharmacologically active molecules. Researchers also employ it to investigate structure-activity relationships (SAR) in phenethylamine derivatives. Its applications extend to in vitro assays for evaluating adrenergic and serotonergic activity.

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