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N-METHYLPHENETHYLAMINE HYDROCHLORIDE, also known as N-methyl-beta-phenylethylamine hydrochloride, is a phenethylamine derivative and a stimulant with adrenergic properties. It is a chemical compound belonging to the class of organic compounds and is related to amphetamine. N-METHYLPHENETHYLAMINE HYDROCHLORIDE has been utilized in pharmaceuticals as a sympathomimetic amine and has garnered interest for its potential in enhancing cognitive function and mood.

4104-43-2

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4104-43-2 Usage

Uses

Used in Pharmaceutical Industry:
N-METHYLPHENETHYLAMINE HYDROCHLORIDE is used as a sympathomimetic amine for its stimulant effects, which can help in treating conditions that require increased alertness or arousal.
Used in Cognitive Function Enhancement:
N-METHYLPHENETHYLAMINE HYDROCHLORIDE is used as a cognitive enhancer for its potential to improve brain function, focus, and memory, making it a candidate for applications in nootropics and treatments for cognitive disorders.
Used in Mood Enhancement:
N-METHYLPHENETHYLAMINE HYDROCHLORIDE is used as a mood elevator for its capacity to elevate mood and potentially alleviate symptoms of depression or other mood-related conditions, based on its stimulant and adrenergic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 4104-43-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,0 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4104-43:
(6*4)+(5*1)+(4*0)+(3*4)+(2*4)+(1*3)=52
52 % 10 = 2
So 4104-43-2 is a valid CAS Registry Number.
InChI:InChI=1S/C9H13N.ClH/c1-10-8-7-9-5-3-2-4-6-9;/h2-6,10H,7-8H2,1H3;1H

4104-43-2Relevant academic research and scientific papers

Efficient synthesis of tertiary amines from secondary amines

Kurosu, Michio,Dey, Sevendu Sekhar,Crick, Dean C.

, p. 4871 - 4875 (2007/10/03)

Reliable N-alkylations of secondary amines have been developed. By using DIAD and TPP (or PS-TPP) a variety of secondary amines can be converted to the corresponding tertiary amines in good to excellent yields with diverse alkylhalides; no formation of quaternary amine salts are observed. These protocols are amenable to combinatorial chemistry libraries, and are also useful for the syntheses of secondary amines by an acid lysis of the cleavable tertiary amino resins.

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