4-methoxyaniline


anisidin; p-anisidine; p-methoxyaniline; 4-methoxyaniline; 4-methoxybenzenamine
Links:📏 NIST, ⚗️ ChemSynthesis, 📖 PubMed,
📖Houben-Weyl, 2. Band (Anisidin); p. 416
CAS:[104-94-9]
Formula:C7H9NO; 123.15 g/mol
InChiKey:BHAAPTBBJKJZER-UHFFFAOYSA-N
SMILES:COc1ccc(N)cc1
Molecular structure of 4-methoxyaniline
Density:1.061 g/mL
Molar volume:116.1 mL/mol
Refractive index:1.556
Molecular refractive power:37.32 mL/mol
Dielectric constant:8.84
Dipole moment:1.80 D
Melting point:57 °C
Boiling point:246 °C
Log10 partition octanol / water:0.95

Isomers

Molecular structure of anilinomethanol
2-acetyl-1-methylpyrrole
Molecular structure of 2-acetyl-1-methylpyrrole
3-acetyl-1-methylpyrrole
Molecular structure of 3-acetyl-1-methylpyrrole
2-aminobenzyl alcohol
Molecular structure of 2-aminobenzyl alcohol
3-aminobenzyl alcohol
Molecular structure of 3-aminobenzyl alcohol
4-aminobenzyl alcohol
Molecular structure of 4-aminobenzyl alcohol
3-amino-2-cresol
Molecular structure of 3-amino-2-cresol
2-amino-3-methylphenol
Molecular structure of 2-amino-3-methylphenol
2-amino-4-methylphenol
Molecular structure of 2-amino-4-methylphenol
2-amino-5-methylphenol
Molecular structure of 2-amino-5-methylphenol
3-amino-4-methylphenol
Molecular structure of 3-amino-4-methylphenol
4-amino-2-methylphenol
Molecular structure of 4-amino-2-methylphenol
4-amino-3-methylphenol
Molecular structure of 4-amino-3-methylphenol
5-amino-2-methylphenol
Molecular structure of 5-amino-2-methylphenol
O-benzylhydroxylamine
Molecular structure of O-benzylhydroxylamine
2-cyanocyclohexanone
Molecular structure of 2-cyanocyclohexanone
cyclohexa-1,3-dienecarbaldehyde oxime
Molecular structure of cyclohexa-1,3-dienecarbaldehyde oxime
2,6-dimethylpyridine N-oxide
Molecular structure of 2,6-dimethylpyridine N-oxide
3,5-dimethylpyridine N-oxide
Molecular structure of 3,5-dimethylpyridine N-oxide
2-ethoxypyridine
Molecular structure of 2-ethoxypyridine
3-ethoxypyridine
Molecular structure of 3-ethoxypyridine
5-hydroxymethyl-2-methylpyridine
Molecular structure of 5-hydroxymethyl-2-methylpyridine
2-methoxyaniline
Molecular structure of 2-methoxyaniline
3-methoxyaniline
Molecular structure of 3-methoxyaniline
4-methoxyaniline
Molecular structure of 4-methoxyaniline
2-(methoxymethyl)pyridine
Molecular structure of 2-(methoxymethyl)pyridine
2-methoxy-4-methylpyridine
Molecular structure of 2-methoxy-4-methylpyridine
2-methoxy-6-methylpyridine
Molecular structure of 2-methoxy-6-methylpyridine
2-methylaminophenol
Molecular structure of 2-methylaminophenol
4-methylaminophenol
Molecular structure of 4-methylaminophenol
2-methyl-3-hydroxymethylpyridine
Molecular structure of 2-methyl-3-hydroxymethylpyridine
1-methyl-2-oxocyclopentanecarbonitrile
Molecular structure of 1-methyl-2-oxocyclopentanecarbonitrile
N-(4-methylphenyl)hydroxylamine
Molecular structure of N-(4-methylphenyl)hydroxylamine
6-methyl-2-pyridinemethanol
Molecular structure of 6-methyl-2-pyridinemethanol
(1R)-1-pyridin-4-ylethanol
Molecular structure of (1R)-1-pyridin-4-ylethanol
(1S)-1-pyridin-4-ylethanol
Molecular structure of (1S)-1-pyridin-4-ylethanol
1-pyridin-4-ylethanol
Molecular structure of 1-pyridin-4-ylethanol
2-pyrid-2-ylethanol
Molecular structure of 2-pyrid-2-ylethanol
2-pyrid-3-ylethanol
Molecular structure of 2-pyrid-3-ylethanol
2-pyrid-4-ylethanol
Molecular structure of 2-pyrid-4-ylethanol
1-(1H-pyrrol-2-yl)propan-1-one
Molecular structure of 1-(1H-pyrrol-2-yl)propan-1-one