65017-65-4 Usage
General Description
(+/-)-2-(3-methoxyphenyl)-1-phenylethylamine, also 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 has similar effects, including increased energy, euphoria, and enhanced sensory perception. It works by increasing the levels of dopamine, serotonin, and norepinephrine in the brain. MDA is a Schedule I controlled substance in the United States and is illegal to manufacture, distribute, or possess without a license. Its recreational use is associated with potential adverse effects such as increased heart rate, elevated blood pressure, and risk of addiction.
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.
65017-65-4Relevant articles and documents
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.
