Interesting facts
Interesting Facts about 1-(3,4-Dichlorophenyl)-2-(isopropylamino)ethanol Hydrochloride
This compound, commonly referred to as a hydrochloride salt, is positioned intriguingly within the realm of medicinal chemistry. Here are some remarkable insights:
- Pharmacological Activity: This compound is known for its action as a selective serotonin reuptake inhibitor (SSRI), which is pivotal in the treatment of various mood disorders and conditions such as depression. SSRIs work by increasing the levels of serotonin, a neurotransmitter that contributes to feelings of well-being and happiness.
- Structural Characteristics: The structure of 1-(3,4-dichlorophenyl)-2-(isopropylamino)ethanol features a dichlorophenyl group. This particular arrangement is essential for its pharmacological effects and demonstrates how subtle modifications to a molecular structure can significantly alter a compound's biological activity.
- Targeting Specific Receptors: The unique characteristics of this molecule allow it to interact selectively with serotonin receptors, emphasizing the importance of receptor specificity in drug design. As a future chemist, understanding these interactions can lead to more effective medicines with fewer side effects.
- Historical Context: The discovery and development of compounds like this have revolutionized mental health treatment since the late 20th century. Although this specific compound might not be widely known, its chemical framework highlights the evolution of antidepressants over the decades.
In summary, 1-(3,4-dichlorophenyl)-2-(isopropylamino)ethanol hydrochloride exemplifies the intricate relationship between chemistry and pharmacology. As scientists and students delve deeper into the study of such compounds, they uncover not just the mechanics of drug action but also the profound impact these substances have on society.
Synonyms
Dichloroisoproterenol hydrochloride
51-29-6
DCI hydrochloride
Compound 20522
Lilly 20522
1-(3',4'-Dichlorophenyl)-2-isopropylaminoethanol hydrochloride
Dichloroisoprenaline hydrochloride
Dichlorisoproterenol hydrochloride
Dichloroisoproterenol HCl
EINECS 200-088-2
NSC 72104
UNII-XD42620PS5
AI3-52113
XD42620PS5
NSC-72104
beta-Hydroxy-N-isopropyl-3,4-dichloro-phenethylamine hydrochloride
DTXSID401018909
Benzenemethanol, 3,4-dichloro-alpha-(((1-methylethyl)amino)methyl)-, hydrochloride
.beta.-Hydroxy-N-isopropyl-3,4-dichloro-phenethylamine hydrochloride
BENZYL ALCOHOL, 3,4-DICHLORO-alpha-((ISOPROPYLAMINO)METHYL)-, HYDROCHLORIDE
(+/-)-DICHLOROISOPROTERENOL HYDROCHLORIDE
BENZENEMETHANOL, 3,4-DICHLORO-.ALPHA.-(((1-METHYLETHYL)AMINO)METHYL)-, HYDROCHLORIDE (1:1)
1-(3,4-dichlorophenyl)-2-(propan-2-ylamino)ethanol hydrochloride
Benzenemethanol, 3,4-dichloro-alpha-[[(1-methylethyl)amino]methyl]-, hydrochloride (1:1)
BENZENEMETHANOL, 3,4-DICHLORO-ALPHA-(((1-METHYLETHYL)AMINO)METHYL)-, HYDROCHLORIDE (1:1)
WLN: GR BG DYQ1MY &GH
DTXCID901476924
NSC72104
3,4-Dichloro-alpha-((isopropylamino)methyl)benzyl alcohol hydrochloride
AKOS024325898
DB-051937
NS00041151
A828521
Q27293789
1-(3,4-Dichlorophenyl)-2-(isopropylamino)ethanol hydrochloride
1-(3,4-dichlorophenyl)-2-(propan-2-ylamino)ethanol;hydrochloride
Benzyl alcohol,4-dichloro-.alpha.-[(isopropylamino)methyl]-, hydrochloride
Benzenemethanol, 3,4-dichloro-alpha-(((1-methylethyl)amino)methyl)-, hydrochloride (9CI)
Benzenemethanol,4-dichloro-.alpha.-[[(1-methylethyl)amino]methyl]-, hydrochloride
200-088-2
Solubility of 1-(3,4-dichlorophenyl)-2-(isopropylamino)ethanol; hydrochloride
The solubility of 1-(3,4-dichlorophenyl)-2-(isopropylamino)ethanol; hydrochloride (C16H22ClNO2) is influenced by its molecular structure and functional groups. Here are some key points regarding its solubility:
In conclusion, while 1-(3,4-dichlorophenyl)-2-(isopropylamino)ethanol; hydrochloride is expected to be soluble in aqueous environments, the presence of specific substituents could also dictate its behavior in varied solvent systems. Overall, understanding the solubility profile is crucial for applications in pharmaceuticals and chemistry.