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(+/-)-2-(3-methoxyphenyl)-1-phenylethylamine, commonly known as 3,4-methylenedioxyamphetamine (MDA), is a psychoactive drug and entactogen. It is a substituted amphetamine and a derivative of phenethylamine. MDA is closely related to MDMA (ecstasy) and exhibits similar effects, such as increased energy, euphoria, and enhanced sensory perception. It functions by increasing the levels of dopamine, serotonin, and norepinephrine in the brain. MDA is classified as a Schedule I controlled substance in the United States, making it illegal to manufacture, distribute, or possess without a license. Its recreational use is associated with potential adverse effects, including increased heart rate, elevated blood pressure, and risk of addiction.

65017-65-4

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65017-65-4 Usage

Uses

Used in Pharmaceutical Research:
(+/-)-2-(3-methoxyphenyl)-1-phenylethylamine is used as a research chemical for studying the effects of psychoactive substances on the brain and their potential therapeutic applications. Its ability to modulate neurotransmitter levels makes it a valuable tool in understanding the mechanisms of action for various mental health conditions and the development of new treatments.
Used in Forensic Toxicology:
In forensic toxicology, (+/-)-2-(3-methoxyphenyl)-1-phenylethylamine is utilized for the identification and analysis of controlled substances in biological samples. This helps in determining the presence of MDA in cases of drug abuse or overdose, aiding in legal proceedings and public health initiatives.
Used in Drug Policy and Regulation:
(+/-)-2-(3-methoxyphenyl)-1-phenylethylamine is used as a reference substance in the development and enforcement of drug policies and regulations. Its classification as a Schedule I controlled substance informs the legal framework surrounding the manufacture, distribution, and possession of psychoactive drugs, ensuring public safety and compliance with international drug control conventions.

Check Digit Verification of cas no

The CAS Registry Mumber 65017-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,1 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65017-65:
(7*6)+(6*5)+(5*0)+(4*1)+(3*7)+(2*6)+(1*5)=114
114 % 10 = 4
So 65017-65-4 is a valid CAS Registry Number.

65017-65-4Upstream product

65017-65-4Relevant academic research and scientific papers

Regiochemistry on Photoamination of Stilbene Derivatives with Ammonia via Electron Transfer

Yasuda, Masahide,Isami, Toshihiro,Kubo, Jun-ichi,Mizutani, Manabu,Yamashita, Toshiaki,et al.

, p. 1351 - 1354 (1992)

The regiochemistry of photoamination of 1,2-diarylethene (1) with ammonia in the presence of p-dicyanobenzene (DCNB) has been investigated.The photoamination of stilbene and p,p'-dimethoxystilbene gave 1-amino-1,2-diphenylethane and 1-amino-1,2-bis(p-methoxyphenyl)ethane, respectively.The photoamination of unsymmetric 1-aryl-2-phenylethene having an alkoxy group on the para position occurred selectively to give 1-amino-2-aryl-1-phenylethane.On the other hand, the photoamination of 1-aryl-2-phenylethene having a methyl and chloro group on the para position or methoxy group on the meta and ortho positions gave both 1-amino-2-aryl-1-phenylethane and 1-amino-1-aryl-2-phenylethane.The regiochemistry is related with the distribution of positive charge in the cation radicals of 1 generated from photochemical electron transfer to DCNB.

Process for producing optically active 3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic acid, and salt thereof

-

, (2008/06/13)

There are disclosed are a diastereomer salt of formula (1): a process for producing the same, a process for producing optically active 3,3,3-trifluoro-2-hydroxy-2-methylpropionic acid of formula (2′): a novel optically active amine compound of formula (4): a novel optically active amine compound of formula (8): an imine compound of formula (7) or (11):

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