50822-98-5 Usage
Uses
Used in Pharmaceutical Research:
N,N-Dimethyl-4-methoxyphenethylamine hydrochloride is utilized as a research chemical for studying its psychoactive properties and potential effects on the central nervous system. Its structural similarity to amphetamines makes it a valuable compound for understanding the mechanisms of action and developing new therapeutic agents for neurological disorders.
Used in Recreational Drug Markets:
Due to its psychoactive properties, N,N-Dimethyl-4-methoxyphenethylamine hydrochloride has found its way into recreational drug markets under the street name "Dimethoxyphenethylamine" (DMPEA). It is used by some individuals for its stimulant and mood-altering effects, although its safety and long-term health implications are not well understood.
Used in Forensic Toxicology:
N,N-Dimethyl-4-methoxyphenethylamine hydrochloride is also employed in forensic toxicology as a reference compound for identifying and analyzing designer drugs in biological samples. This aids in the detection and monitoring of drug abuse and the development of new analytical methods for drug screening.
Check Digit Verification of cas no
The CAS Registry Mumber 50822-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,8,2 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50822-98:
(7*5)+(6*0)+(5*8)+(4*2)+(3*2)+(2*9)+(1*8)=115
115 % 10 = 5
So 50822-98-5 is a valid CAS Registry Number.
50822-98-5Relevant academic research and scientific papers
Compound 48/80. Structure activity relations and poly THIQ, a new, more potent analog
Read,Kiefer,Weber
, p. 1292 - 1295 (2007/10/04)
Derivatives of p methoxyphenethylmethylamine were synthesized from which formaldehyde copolymers analogous to compound 48/80 were prepared. Measurement of the hypotensive activity of these analogs revealed that potency was not enhanced by changing the group in the para position, by varying the length of the alkyl group, or by altering the degree of methylation of the amine. However, when the ethylamine side chain was cyclized to form 7 methoxytetrahydroisoquinoline, the copolymer prepared from this derivative (poly THIQ) was seven times more potent than compound 48/80. The hypotensive action of poly THIQ was found to result from the liberation of histamine, as with compound 48/80.
