Interesting facts
Insights into 4-[2-(dimethylamino)-1-hydroxy-ethyl]benzene-1,2-diol
This compound, often referred to in the context of various pharmacological applications, showcases a fascinating molecular structure that combines both aromatic and aliphatic components. Here are some engaging facts about 4-[2-(dimethylamino)-1-hydroxy-ethyl]benzene-1,2-diol:
- Dual Functionality: The presence of both a benzene ring and an alcohol group means this compound can participate in both electrophilic substitution and hydrogen bonding reactions, making it versatile in synthetic applications.
- Biological Relevance: Its structure includes a dimethylamino group, which is known to enhance biological activity by increasing lipophilicity and improving membrane permeability.
- Potential Therapeutic Uses: Compounds with similar structures have been studied for their roles in pharmaceuticals, especially as potential agents in treating various diseases due to their ability to interact with biological receptors.
- Synthetic Pathways: The synthesis of this compound provides insights into organic reaction mechanisms, particularly nucleophilic substitutions and the role of protecting groups in complex organic synthesis.
- Analytical Techniques: To identify and characterize this compound, chemists often utilize advanced techniques like NMR spectroscopy and mass spectrometry, which can reveal underlying structural features.
In conclusion, 4-[2-(dimethylamino)-1-hydroxy-ethyl]benzene-1,2-diol not only emphasizes the rich connection between structure and function in chemistry but also opens doors to intriguing discussions about its applications in the field of medicinal chemistry. As one scholar famously stated, “In the world of chemistry, the smallest differences in structure can lead to the most significant variations in function.”
Synonyms
N-Methylepinephrine
Methadrene
N-Methyladrenaline
554-99-4
dl-N-Methylepinephrine
NSC 169812
EINECS 209-078-2
UNII-T12BO931W4
METHADREN(E)
T12BO931W4
alpha-(Dimethylaminomethyl)protocatechuyl alcohol
NSC-169812
alpha-(3,4-Dihydroxyphenyl)-beta-dimethylaminoethanol
Protocatechuyl alcohol, alpha-((dimethylamino)methyl)-
3,4-Dihydroxy-alpha-(dimethylaminomethyl) benzyl alcohol
3,4-Dihydroxy-alpha-(dimethylaminomethyl)benzyl alcohol
1,2-Benzenediol, 4-(2-(dimethylamino)-1-hydroxyethyl)-
alpha-(3,4-Dihydroxyphenyl)-alpha-hydroxy-beta-dimethylaminoethane
.alpha.-(Dimethylaminomethyl)protocatechuyl alcohol
.alpha.-(3,4-Dihydroxyphenyl)-.beta.-dimethylaminoethanol
1,2-Benzenediol, 4-[2-(dimethylamino)-1-hydroxyethyl]-
3,4-Dihydroxy-.alpha.-(dimethylaminomethyl)benzyl alcohol
N-METHYLEPINEPHRINE DL-FORM [MI]
BENZYL ALCOHOL, alpha-((DIMETHYLAMINO)METHYL)-3,4-DIHYDROXY-
.alpha.-(3,4-Dihydroxyphenyl)-.alpha.-hydroxy-(.beta.-dimethylamino)ethane
Protocatechuyl alcohol, .alpha.-((dimethylamino)methyl)-
Benzyl alcohol, .alpha.-((dimethylamino)methyl)-3,4-dihydroxy-
1,2-BENZENEDIOL, 4-(2-(DIMETHYLAMINO)-1-HYDROXYETHYL)-)
N-METHYLEPINEPHRINE DL-FORM
alpha((dimethylamino)methyl)-3,4-dihydroxybenzyl alcohol
1,2-Benzenediol, 4-(2-(dimethylamino)-1-hydroxyethyl)-(9CI)
alpha-(3,4-Dihydroxyphenyl)-alpha-hydroxy-(beta-dimethylamino)ethane
209-078-2
rlatyncitholtj-uhfffaoysa-n
4-[2-(dimethylamino)-1-hydroxyethyl]benzene-1,2-diol
4-[2-(DIMETHYLAMINO)-1-HYDROXYETHYL]PYROCATECHOL
4-(2-(Dimethylamino)-1-hydroxyethyl)pyrocatechol
rac N-Methyl Epinephrine
Benzyl alcohol,4-dihydroxy-
SCHEMBL521779
WLN: QR BQ DYQ1N1&1
DTXSID50871762
NSC169812
DB-228803
1, 4-[2-(dimethylamino)-1-hydroxyethyl]-
NS00044049
.alpha.-[(dimethylamino)methyl]protocatechuyl alcohol
4-(2-Dimethylamino-1-hydroxyethyl)benzene-1,2-diol
Q27289528
4-[2-(Dimethylamino)-1-hydroxyethyl]-1,2-benzenediol #
.alpha.-(3,4-Dihydroxyphenyl)-(.beta.-dimethylamino)ethanol
3,4-Dihydroxy-.alpha.-[(dimethylamino)methyl] benzyl alcohol
benzene, 1-(2-dimethylamino-1-hydroxy)ethyl-3,4-dihydroxy-
Solubility of 4-[2-(dimethylamino)-1-hydroxy-ethyl]benzene-1,2-diol
The solubility of 4-[2-(dimethylamino)-1-hydroxy-ethyl]benzene-1,2-diol is influenced by its chemical structure, particularly the presence of both hydrophilic and hydrophobic groups. This compound features a benzene ring with hydroxyl groups, which generally enhance solubility in polar solvents such as water.
Some key factors affecting its solubility include:
In general, while 4-[2-(dimethylamino)-1-hydroxy-ethyl]benzene-1,2-diol is likely to be soluble in polar solvents, its solubility can be significantly reduced in non-polar environments. As the old adage goes, "like dissolves like," and this holds true for this compound as well.
Overall, understanding the balance between hydrophilic and hydrophobic characteristics in chemical compounds is essential for predicting their solubility in various solvents.