5344-61-6 Usage
Description
1-(2-methoxyphenyl)propan-2-amine, also known as 2-Methoxyamphetamine (2-MA), is a psychoactive drug and research chemical belonging to the amphetamine and phenethylamine classes. It is a synthetic compound with stimulant properties, acting as a releasing agent for serotonin, norepinephrine, and dopamine.
Used in Pharmaceutical Industry:
1-(2-methoxyphenyl)propan-2-amine is used as a research chemical for studying the effects and mechanisms of action of stimulant drugs on the central nervous system. Its psychoactive properties and interactions with neurotransmitters make it a subject of interest for scientific investigation.
Note: Due to the potential for abuse, adverse health effects, and legal restrictions associated with 1-(2-methoxyphenyl)propan-2-amine, its recreational use is strongly discouraged. The information provided is for educational purposes only and does not endorse or promote the use of this substance.
Check Digit Verification of cas no
The CAS Registry Mumber 5344-61-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5344-61:
(6*5)+(5*3)+(4*4)+(3*4)+(2*6)+(1*1)=86
86 % 10 = 6
So 5344-61-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H13Cl2NO2S/c16-12-7-8-13(17)15(10-12)21(19,20)18-9-3-5-11-4-1-2-6-14(11)18/h1-2,4,6-8,10H,3,5,9H2
5344-61-6Relevant articles and documents
Co-Catalyzed Synthesis of Primary Amines via Reductive Amination employing Hydrogen under very mild Conditions
Elfinger, Matthias,Sch?nauer, Timon,Thom?, Sabrina L. J.,St?glich, Robert,Drechsler, Markus,Zobel, Mirijam,Senker, Jürgen,Kempe, Rhett
, p. 2360 - 2366 (2021/05/03)
Nanostructured and reusable 3d-metal catalysts that operate with high activity and selectivity in important chemical reactions are highly desirable. Here, a cobalt catalyst was developed for the synthesis of primary amines via reductive amination employing hydrogen as the reducing agent and easy-to-handle ammonia, dissolved in water, as the nitrogen source. The catalyst operates under very mild conditions (1.5 mol% catalyst loading, 50 °C and 10 bar H2 pressure) and outperforms commercially available noble metal catalysts (Pd, Pt, Ru, Rh, Ir). A broad scope and a very good functional group tolerance were observed. The key for the high activity seemed to be the used support: an N-doped amorphous carbon material with small and turbostratically disordered graphitic domains, which is microporous with a bimodal size distribution and with basic NH functionalities in the pores.