2-[(4-Methoxybenzyl)amino]ethanol hydrochloride
CAS No.:
100132-03-4
M. Wt:
217.69254
M. Fa:
C10H16ClNO2
InChI Key:
TVKAJTZWKWAXKX-UHFFFAOYSA-N
Names and Identifiers of 100132-03-4
CAS Number |
100132-03-4 |
|---|---|
MDL Number |
MFCD07108562 |
IUPAC Name |
2-[(4-methoxyphenyl)methylamino]ethanol;hydrochloride |
InChI |
InChI=1S/C10H15NO2.ClH/c1-13-10-4-2-9(3-5-10)8-11-6-7-12;/h2-5,11-12H,6-8H2,1H3;1H |
InChIKey |
TVKAJTZWKWAXKX-UHFFFAOYSA-N |
Canonical SMILES |
COC1=CC=C(C=C1)CNCCO.Cl |
UNSPSC Code |
12352100 |
Physical and chemical properties of 100132-03-4
Molecular Formula |
C10H16ClNO2 |
|---|---|
Molecular Weight |
217.69254 |
Safety Information of 100132-03-4
Applications of 100132-03-4
2-[(4-Methoxybenzyl)amino]ethanol hydrochloride has several applications, particularly in:
- Pharmaceuticals: It serves as an intermediate in drug synthesis or as a reference standard for analytical studies.
- Biochemical research: Its unique structure makes it useful in studying enzyme interactions and metabolic pathways.
- Cosmetics: Due to its potential antimicrobial properties, it may be incorporated into formulations aimed at skin health.
These applications highlight its versatility in both research and commercial products.
Interaction Studies of 100132-03-4
Interaction studies involving 2-[(4-Methoxybenzyl)amino]ethanol hydrochloride have focused on:
- Drug-drug interactions: Investigating how this compound interacts with other pharmaceuticals, particularly those affecting neurotransmitter systems.
- Biomolecular interactions: Analyzing how it binds to proteins or enzymes, which is crucial for understanding its mechanism of action.
Such studies are vital for assessing safety profiles and therapeutic efficacy.
Biological Activity of 100132-03-4
Research indicates that 2-[(4-Methoxybenzyl)amino]ethanol hydrochloride exhibits notable biological activities. It has been studied for its potential as:
- Antidepressant: Preliminary studies suggest that it may influence neurotransmitter systems, contributing to mood regulation.
- Antimicrobial agent: Its structural components may provide activity against certain bacterial strains.
- Neuroprotective effects: There is evidence that this compound could protect neuronal cells from oxidative stress.
These activities make it a candidate for further pharmacological studies aimed at developing new therapeutic agents.
