CAS 14489-75-9

N-Methyl-1-naphthalenemethanamine

Description:

N-Methyl-1-naphthalenemethanamine, also known as N-Methyl-1-naphthylmethanamine, is an organic compound characterized by its naphthalene structure, which consists of two fused aromatic rings. This compound features a methyl group attached to the nitrogen atom of the amine, enhancing its lipophilicity. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. N-Methyl-1-naphthalenemethanamine is known for its potential applications in various fields, including pharmaceuticals and organic synthesis, where it may serve as an intermediate or building block. The presence of the naphthalene moiety contributes to its aromatic properties, which can influence its reactivity and interactions with other chemical species. Additionally, this compound may exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance. Overall, N-Methyl-1-naphthalenemethanamine is a notable compound within the realm of organic chemistry.

Formula: C₁₂H₁₃N

InChI: InChI=1S/C12H13N/c1-13-9-11-7-4-6-10-5-2-3-8-12(10)11/h2-8,13H,9H2,1H3

InChI key: InChIKey=MQRIUFVBEVFILS-UHFFFAOYSA-N

SMILES: C(NC)C=1C2=C(C=CC1)C=CC=C2

Synonyms:

• (1-Naphthylmethyl)Methylamine Hydrochloride
• 1-(1-Naphthalenyl)Methylamine
• 1-(Methylaminomethyl)Naphthalene
• 1-Methyl-1-Naphthalenemethylamine
• 1-Methyl-Aminomethyl-1-Naphthalene
• 1-Methyl-Aminomethylnaphthalene
• 1-Methylaminomethylnaphthalene
• 1-Naphthalenemethanamine, N-methyl-
• 1-Naphthalenemethylamine, N-methyl-
• Aurora Ka-7760
• Methyl(1-naphthylmethyl)amine
• Methyl(naphthalen-1-ylmethyl)amine
• N-(1-Naphthylmethyl)methylamine
• N-(Naphthalen-1-yl-methyl)-N-methylamine
• N-Methyl Hydrochloric Salt
• N-Methyl Naphthylmethylamine
• N-Methyl-1-Naphthalene Methylamine
• N-Methyl-1-Naphthalenemethyl Amine
• N-Methyl-1-Naphthalenemethylamine
• N-Methyl-1-Naphthylmethylamine
• N-Methyl-1-naphthalenemethanamine
• N-Methyl-N-[(1-naphthyl)methyl]amine
• N-Methyl-N-[(naphthalen-1-yl)methyl]amine
• N-Methyl-N-naphthylmethylamine
• N-Methylnaphthalene-1-Methylamine
• N-methyl-1-(naphthalen-1-yl)methanamine
• N-methyl-1-napthylmethylamine
• NSC 129392
• Timtec-Bb Sbb005765
• [(Naphthalen-1-yl)methyl]methylamine

N-Methyl-1-naphthylmethylamine

CAS: 14489-75-9

Formula: C₁₂H₁₃N

Purity: >98.0%(T)

Color and Shape: Colorless to Orange to Green clear liquid

Molecular weight: 171.24

Ref: 3B-M0983

1-Naphthalenemethanamine, N-methyl-

CAS: 14489-75-9

Formula: C₁₂H₁₃N

Purity: 95%

Color and Shape: Liquid

Molecular weight: 171.2383

Ref: IN-DA001KAY

1-Methyl-Aminomethyl Naphthalene

CAS: 14489-75-9

1-Methyl-Aminomethyl Naphthalene

Purity: 98%

Molecular weight: 171.24g/mol

Ref: 54-OR1009537

Methyl-1-naphthalenemethylamine

CAS: 14489-75-9

Impurity Terbinafine EP Impurity A; Terbinafine BP Impurity A; Terbinafine USP Related Compound A
Applications Terbinafine EP Impurity A. Terbinafine BP Impurity A. Terbinafine USP Related Compound A

Formula: C₁₂H₁₃N

Color and Shape: Orange

Molecular weight: 171.24

Ref: TR-M323140

Terbinafine EP Impurity A

CAS: 14489-75-9

Formula: C₁₂H₁₃N

Molecular weight: 171.24

Ref: ST-EA-CP-T34001

n-Methylnaphthalene-1-methylamine

CAS: 14489-75-9

Formula: C₁₂H₁₃N

Purity: 95%

Color and Shape: Liquid

Molecular weight: 171.243

Ref: 10-F013168

Methyl-1-naphthalenemethylamine

CAS: 14489-75-9

Methyl-1-naphthalenemethylamine is a synthetic drug that is used as an anti-fungal agent. It is used to treat dermatophytosis and onychomycosis caused by Trichophyton mentagrophytes. Methyl-1-naphthalenemethylamine has been shown to have a clinical response in patients with the skin condition tinea pedis. This drug inhibits the growth of fungi by inhibiting cell membrane synthesis, which leads to cell death. Methyl-1-naphthalenemethylamine has been shown to be effective against Trichophyton mentagrophytes in plasma samples from patients with tinea pedis who were treated with this drug. The effectiveness of this drug may be due to its ability to inhibit the synthesis of polysaccharides, proteins, and lipids in the fungal cell membrane, or its ability to inhibit protein synthesis by binding with ribos

Formula: C₁₂H₁₃N

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 171.24 g/mol

Ref: 3D-FM25618