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(R)-(+)-1-(4-Methylphenyl)ethylamine hydrochloride, also known as para-methylamphetamine, is a psychoactive chemical compound belonging to the amphetamine class. It acts as a central nervous system stimulant and has potential for abuse. This hydrochloride salt form is more stable and water-soluble, making it suitable for various experimental applications in research settings.

404336-49-8

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404336-49-8 Usage

Uses

Used in Research Settings:
(R)-(+)-1-(4-Methylphenyl)ethylamine hydrochloride is used as a reference standard or starting material for the synthesis of other compounds in research settings. It aids in the development and understanding of new substances and their properties.
Used in Medical Research:
In the field of medical research, (R)-(+)-1-(4-Methylphenyl)ethylamine hydrochloride is used to study the effects of amphetamine derivatives on the brain and behavior. This helps in understanding the mechanisms of action and potential therapeutic applications of these substances.
Regulatory Considerations:
Due to its potential for misuse and dependence, the use of (R)-(+)-1-(4-Methylphenyl)ethylamine hydrochloride is tightly regulated to ensure its application is limited to legitimate research and medical purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 404336-49-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,3,3 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 404336-49:
(8*4)+(7*0)+(6*4)+(5*3)+(4*3)+(3*6)+(2*4)+(1*9)=118
118 % 10 = 8
So 404336-49-8 is a valid CAS Registry Number.

404336-49-8Upstream product

404336-49-8Downstream Products

404336-49-8Relevant academic research and scientific papers

Enantioselective hydrogenation of N-H imines

Hou, Guohua,Gosselin, Francis,Li, Wei,McWilliams, J. Christopher,Sun, Yongkui,Weisel, Mark,O'Shea, Paul D.,Chen, Cheng-Yi,Davies, Ian W.,Zhang, Xumu

supporting information; experimental part, p. 9882 - 9883 (2009/12/06)

(Figure Presented) N-H ketoimines 3a-3v are readily prepared in high yield via organometallic addition to nitriles and isolated as corresponding bench-stable hydrochloride salts. Homogeneous asymmetric hydrogenation of unprotected N-H ketoimines 3a-3v usi

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