854184-18-2 Usage
Chemical structure
The compound consists of a hydrochloride salt of ethylamine with a 3-methoxyphenyl group attached.
Common use
It is commonly used in research and drug development as a precursor to various pharmaceuticals and organic compounds.
Potential applications
It may have potential applications in the field of neuroscience and psychiatric medicine due to its ability to interact with neurotransmitter systems in the brain.
Use as a reagent
It may have use as a reagent in chemical synthesis and as an intermediate in the production of other organic compounds.
Precautions
Proper handling, storage, and disposal procedures should be followed to minimize the risk of exposure and potential harm to individuals and the environment.
Regulatory status
Depending on the jurisdiction, 1-(3-Methoxyphenyl)ethylamine hydrochloride may be subject to regulatory controls and restrictions related to its use, distribution, and disposal.
Purity
The purity of the compound can affect its performance and safety, so it is essential to ensure that it meets the required specifications for its intended use.
Stability
The compound may be sensitive to certain environmental conditions, such as temperature, humidity, and light, which can affect its stability and performance.
Synonyms
It may be known by different names or synonyms, depending on the context in which it is used or the specific application for which it is intended.
Check Digit Verification of cas no
The CAS Registry Mumber 854184-18-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,4,1,8 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 854184-18:
(8*8)+(7*5)+(6*4)+(5*1)+(4*8)+(3*4)+(2*1)+(1*8)=182
182 % 10 = 2
So 854184-18-2 is a valid CAS Registry Number.
854184-18-2Relevant academic research and scientific papers
Synthesis and SAR Studies of Isoquinoline and Tetrahydroisoquinoline Derivatives as Melatonin Receptor Ligands
Ettaoussi, Mohamed,Laversin, Amélie,Vreulz, Brandon,Rami, Marouane,Lebegue, Nicolas,Delagrange, Philippe,Caignard, Daniel Henri,Melnyk, Patricia,Liberelle, Maxime,Yous, Sa?d
, (2021/12/03)
In our constant search for new successors of agomelatine, we report herein a new series of compounds resulting from bioisosteric modulation of the naphthalene ring. The isoquinoline and tetrahydroisoquinoline derivatives were synthesized and pharmacologic
