15205-27-3 Usage
General Description
N-(1,3-benzodioxol-5-ylmethyl)-N-methylamine, also known as MDA, is a psychoactive substance that belongs to the amphetamine class of drugs. It is a derivative of 3,4-methylenedioxyamphetamine (MDA) and has stimulating and hallucinogenic effects. MDA is commonly used as a recreational drug, and it is known for its ability to produce feelings of euphoria, increased energy, and altered perception. However, it also carries potential risks of adverse effects on the cardiovascular system and mental health. MDA is considered a controlled substance in many countries and is illegal to possess and distribute without proper authorization.
Check Digit Verification of cas no
The CAS Registry Mumber 15205-27-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,0 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15205-27:
(7*1)+(6*5)+(5*2)+(4*0)+(3*5)+(2*2)+(1*7)=73
73 % 10 = 3
So 15205-27-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2/c1-10-5-7-2-3-8-9(4-7)12-6-11-8/h2-4,10H,5-6H2,1H3/p+1
15205-27-3Relevant articles and documents
Selective synthesis of mono- and di-methylated amines using methanol and sodium azide as C1 and N1 sources
Chakrabarti, Kaushik,Mishra, Anju,Panja, Dibyajyoti,Paul, Bhaskar,Kundu, Sabuj
supporting information, p. 3339 - 3345 (2018/07/29)
A Ru(ii) complex mediated synthesis of various N,N-dimethyl and N-monomethyl amines from organic azides using methanol as a methylating agent is reported. This methodology was successfully applied for a one-pot reaction of bromide derivatives and sodium azide in methanol. Notably, by controlling the reaction time several N-monomethylated and N,N-dimethylated amines were synthesized selectively. The practical applicability of this tandem process was revealed by preparative scale reactions with different organic azides and synthesis of an anti-vertigo drug betahistine. Several kinetic experiments and DFT studies were carried out to understand the mechanism of this transformation.
