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(S)-3-methoxy-3-oxo-2-phenylpropan-1-aminium chloride, commonly known as methylephedrine, is a chemical compound classified under the amine class. It is a derivative of ephedrine and is characterized by its central nervous system stimulant properties. Structurally, it closely resembles amphetamine, which raises concerns about its potential for abuse. The chloride salt form of (S)-3-methoxy-3-oxo-2-phenylpropan-1-aminium chloride enhances its solubility and stability, making it more suitable for pharmaceutical applications.

909397-88-2

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909397-88-2 Usage

Uses

Used in Pharmaceutical Industry:
Methylephedrine is used as a nasal decongestant and bronchodilator, providing relief from nasal congestion and aiding in the treatment of respiratory conditions by relaxing the muscles in the airways. Its stimulant properties also contribute to its effectiveness in these applications.
Used in Regulatory Control:
Due to its potential for misuse and abuse, similar to other stimulants like amphetamine, methylephedrine is regulated by many countries. Its legal use may require a prescription to ensure that it is used responsibly and under medical supervision.

Check Digit Verification of cas no

The CAS Registry Mumber 909397-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,3,9 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 909397-88:
(8*9)+(7*0)+(6*9)+(5*3)+(4*9)+(3*7)+(2*8)+(1*8)=222
222 % 10 = 2
So 909397-88-2 is a valid CAS Registry Number.

909397-88-2Upstream product

909397-88-2Relevant academic research and scientific papers

Enantioselective Synthesis of α-Aryl-β2-Amino-Esters by Cooperative Isothiourea and Br?nsted Acid Catalysis

Zhao, Feng,Shu, Chang,Young, Claire M.,Carpenter-Warren, Cameron,Slawin, Alexandra M. Z.,Smith, Andrew D.

, p. 11892 - 11900 (2021)

The synthesis of α-aryl-β2-amino esters through enantioselective aminomethylation of an arylacetic acid ester in high yields and enantioselectivity via cooperative isothiourea and Br?nsted acid catalysis is demonstrated. The scope and limitatio

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