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5-(2-aminoethyl)-2-methoxyphenol

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Identification
Molecular formula
C9H13NO2
CAS number
5672-83-7
IUPAC name
5-(2-aminoethyl)-2-methoxy-phenol
State
State

The compound is typically in a solid state at room temperature.

Melting point (Celsius)
104.00
Melting point (Kelvin)
377.00
Boiling point (Celsius)
307.00
Boiling point (Kelvin)
580.00
General information
Molecular weight
167.20g/mol
Molar mass
167.2200g/mol
Density
1.1403g/cm3
Appearence

5-(2-Aminoethyl)-2-methoxyphenol appears as a white to pale yellow crystalline powder. It may have a slight aromatic odor.

Comment on solubility

Solubility of 5-(2-aminoethyl)-2-methoxy-phenol

The compound 5-(2-aminoethyl)-2-methoxy-phenol, with the chemical formula C9H13NO2, exhibits notable solubility characteristics that can be influenced by various factors.

In general, this compound is known to be:

  • Soluble in polar solvents: Due to the presence of the amino group and the methoxy group, 5-(2-aminoethyl)-2-methoxy-phenol tends to dissolve well in water and alcohols.
  • Insoluble in non-polar solvents: Its structure, particularly the aromatic ring, limits its solubility in non-polar environments like hydrocarbons.
  • pH-dependent: The solubility can be significantly affected by the pH of the solution. At lower pH levels, the amino group can be protonated, increasing its solubility in aqueous media.

In conclusion, the solubility behavior of 5-(2-aminoethyl)-2-methoxy-phenol highlights the influence of functional groups and environmental conditions. As stated, "like dissolves like", emphasizing the importance of polarity in solubility.

Interesting facts

Interesting Facts about 5-(2-Aminoethyl)-2-methoxy-phenol

5-(2-Aminoethyl)-2-methoxy-phenol, often regarded as a fascinating compound, exhibits a variety of intriguing characteristics that make it a subject of study in both organic chemistry and pharmacology. Here are some noteworthy aspects:

  • Biological Significance: This compound possesses structural features that are common in biologically active molecules, suggesting potential roles in pharmacological activities.
  • Structure-Activity Relationship: The presence of the aminoethyl group and the methoxy substituent can influence the compound's interaction with biological targets, providing insight into its mechanism of action.
  • Versatility: The unique combination of functional groups in 5-(2-aminoethyl)-2-methoxy-phenol allows it to participate in various chemical reactions, making it a useful precursor in organic synthesis.
  • Research Interest: Studies have suggested its potential applications in fields such as medicinal chemistry, where compounds with similar structures are explored for therapeutic benefits.
  • Analytical Techniques: Characterizing this compound can involve sophisticated methods like NMR spectroscopy and mass spectrometry, showcasing the analytical skills of chemists.

In conclusion, 5-(2-aminoethyl)-2-methoxy-phenol represents a molecule that bridges the gap between chemical properties and biological activity, making it a compelling topic for continued research and investigation in the chemical sciences.

Synonyms
5-(2-Aminoethyl)-2-methoxyphenol
3213-30-7
4-O-methyldopamine
3-Hydroxy-4-methoxyphenethylamine
Phenol, 5-(2-aminoethyl)-2-methoxy-
4-methoxytyramine
P-METHOXYDOPAMINE
4-METHOXYDOPAMINE
5-(2-AMINO-ETHYL)-2-METHOXY-PHENOL
4-METHOXY-M-TYRAMINE
62MI76A89G
3-hydroxy-4-methoxyphenylethylamine
4-Methoxy-3-hydroxyphenethylamine hydrochloride
Lopac-H-3132
MFCD00044603
DOPAMINE IMPURITY A
5-(2-aminoethyl)-2-(methyloxy)phenol
CHEBI:89641
DTXSID90954003
2-(3-HYDROXY-4-METHOXYPHENYL)ETHYLAMINE
5-hydroxy-4-methoxy-Benzeneethanamine
GUAIACOL, 5-(2-AMINOETHYL)-
DOPAMINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]
DOPAMINE HYDROCHLORIDE IMPURITY A (EP IMPURITY)
UNII-62MI76A89G
Lopac0_000574
SCHEMBL347613
CHEMBL1492473
4-Methoxy-3-hydroxyphenethylamine
DTXCID301382038
4-methoxy-3-hydroxyphenylethylamine
DAA21330
3-hydroxy-4-methoxy-Benzeneethanamine
5-(2-Aminoethyl)-2-methoxyphenol #
AKOS000163417
CCG-204663
Benzeneethanamine, 3-hydroxy-4-methoxy-
Benzeneethanamine, 5-hydroxy-4-methoxy-
NCGC00015505-01
NCGC00015505-02
NCGC00015505-03
NCGC00162191-01
NCGC00162191-02
LS-13654
PD166073
SY184603
DB-349588
EN300-58688
Q27161836
861-848-2