231616-87-8 Usage
Description
Benzenemethanamine, 2,5-dimethoxy-a-methyl-, (aR)-, commonly known as 2C-AM, is a psychoactive drug belonging to the amphetamine class. It is a hallucinogenic substance that can induce euphoria, visual and auditory hallucinations, and altered perception of time and space.
Used in Pharmaceutical Industry:
Used in Research and Development:
Benzenemethanamine, 2,5-dimethoxy-a-methyl-, (aR)is used as a research tool in the study of psychopharmacology and the effects of hallucinogenic substances on the human brain. This helps scientists to better understand the mechanisms of action and potential therapeutic applications of such compounds.
It is crucial to emphasize that Benzenemethanamine, 2,5-dimethoxy-a-methyl-, (aR)is a Schedule I controlled substance in the United States, making it illegal to manufacture, distribute, or possess for any purpose other than research under strict regulations.
Check Digit Verification of cas no
The CAS Registry Mumber 231616-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,1,6,1 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 231616-87:
(8*2)+(7*3)+(6*1)+(5*6)+(4*1)+(3*6)+(2*8)+(1*7)=118
118 % 10 = 8
So 231616-87-8 is a valid CAS Registry Number.
231616-87-8Relevant articles and documents
Design, synthesis, and optical resolution of a novel non-natural chiral auxiliary, 1-(2,5-dimethoxyphenyl)ethylamine. Application to diastereoselective alkylation of aldimines
Kohara, Takehiro,Hashimoto, Yukihiko,Saigo, Kazuhiko
, p. 6453 - 6464 (2007/10/03)
A chiral amine; 1-(2,5-dimethoxyphenyl)ethylamine, was found to be an effective chiral auxiliary for the diastereoselective alkylation of its aldimines with alkylmetals. The 1-(2,5-dimethoxyphenyl)ethyl group of the chiral auxiliary could be removed by the acetylation and then oxidation of the resultant alkylated product, accompanying an amino-transfer from the chiral auxiliary to the final product. Racemic 1-(2,5- dimethoxyphenyl)ethylamine could be easily synthesized from 1,4- dimethoxybenzene and resolved by the diastereomeric salt formation with mandelic acid to give both enantiomers in pure forms.
