CAS 923013-67-6
:4-Ethyl-2,5-dimethoxybenzeneethanamine hydrochloride
Description:
4-Ethyl-2,5-dimethoxybenzeneethanamine hydrochloride, identified by its CAS number 923013-67-6, is a chemical compound that belongs to the class of substituted phenethylamines. This substance features a benzene ring with two methoxy groups and an ethyl substituent, contributing to its unique structural characteristics. The presence of an ethanamine functional group indicates that it has amine properties, which can influence its reactivity and interaction with biological systems. As a hydrochloride salt, it is typically more soluble in water, enhancing its potential applications in various fields, including pharmaceuticals and research. The compound may exhibit psychoactive properties, similar to other phenethylamines, but specific pharmacological effects would depend on its interaction with neurotransmitter systems. Safety and handling precautions are essential, as with many chemical substances, due to potential toxicity or regulatory considerations. Further research is necessary to fully understand its properties, potential applications, and safety profile.
Formula:C12H19NO2.HCl
Synonyms:- Benzeneethanamine,4-ethyl-2,5-dimethoxy-, hydrochloride (1:1)
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
4-Ethyl-2,5-dimethoxyphenethylamine Hydrochloride
CAS:Controlled ProductFormula:C12H19NO2·ClHColor and Shape:NeatMolecular weight:245.754-Ethyl-2,5-dimethoxy-benzeneethanamineHydrochloride
CAS:Controlled Product<p>4-Ethyl-2,5-dimethoxy-benzeneethanamineHydrochloride is a metabolic substrate of CYP2D6. It is also an inhibitor of CYP1A2 and CYP3A4. The class of 4-Ethyl-2,5-dimethoxy-benzeneethanamineHydrochloride is not yet known. 4-Ethyl-2,5-dimethoxy-benzeneethanamineHydrochloride has been shown to cause toxicity in animal studies. Toxicity may be due to its inhibition of cytochrome P450 enzymes, which are involved in metabolism and detoxification.</p>Formula:C12H20ClNO2Purity:Min. 95%Molecular weight:245.75 g/mol

