CAS 2216-67-3
:N-methylnaphthalen-2-amine
Description:
N-methylnaphthalen-2-amine, with the CAS number 2216-67-3, is an organic compound characterized by its structure, which consists of a naphthalene ring substituted with an amino group and a methyl group. This compound typically appears as a solid at room temperature and is known for its aromatic properties due to the presence of the naphthalene moiety. It is a derivative of naphthalene, which contributes to its hydrophobic characteristics. N-methylnaphthalen-2-amine is soluble in organic solvents but has limited solubility in water, reflecting its non-polar nature. The amino group can participate in hydrogen bonding, which may influence its reactivity and interactions with other chemical species. This compound is of interest in various fields, including organic synthesis and materials science, due to its potential applications in dyes, pharmaceuticals, and as an intermediate in chemical manufacturing. Safety precautions should be observed when handling this substance, as it may pose health risks if inhaled or ingested.
Formula:C11H11N
InChI:InChI=1/C11H11N/c1-12-11-7-6-9-4-2-3-5-10(9)8-11/h2-8,12H,1H3
SMILES:CNc1ccc2ccccc2c1
Synonyms:- 2-naphthalenamine, N-methyl-
- N-Methyl-2-naphthalenamine
- N-methyl-N-2-naphthylamine
- N-Methylnaphthalen-2-amine
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Found 3 products.
N-Methylnaphthalen-2-amine
CAS:Formula:C11H11NPurity:95%Color and Shape:LiquidMolecular weight:157.2117N-Methylnaphthalen-2-amine
CAS:<p>N-Methylnaphthalen-2-amine is a metabolite of 2-naphthylamine that is excreted in the urine. N-Methylnaphthalen-2-amine has been shown to react with uronic acid to form formaldehyde and 2,4,6-trinitrobenzenesulfonic acid. This reaction can be used as a test for aromatic amines in urine. The metabolites of this substance are excreted in the urine and conjugated with glucuronic acid or sulfate.</p>Formula:C11H11NPurity:Min. 95%Molecular weight:157.21 g/mol
