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1-(4-methoxyphenyl)pentan-1-amine, also known as 4-MPD, is a research chemical belonging to the cathinone class. It is a psychoactive substance with stimulant effects on the central nervous system, known for its ability to increase energy levels, improve focus and concentration, and enhance mood. 4-MPD is often used for recreational purposes by individuals seeking a euphoric and mentally stimulating experience. However, it also carries potential health risks, including increased heart rate, elevated blood pressure, and anxiety. Its long-term effects on human health are not well-studied, and its use is not sanctioned by regulatory authorities for medical or therapeutic purposes. Caution is advised when dealing with this chemical.

83948-36-1

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83948-36-1 Usage

Uses

Used in Recreational Applications:
1-(4-methoxyphenyl)pentan-1-amine is used as a recreational substance for its ability to increase energy levels, improve focus and concentration, and enhance mood. It provides a euphoric and mentally stimulating experience for individuals seeking such effects.
Used in Research Applications:
1-(4-methoxyphenyl)pentan-1-amine is used as a research chemical in the study of the cathinone class and its effects on the central nervous system. This helps scientists understand the mechanisms of action and potential risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 83948-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,4 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83948-36:
(7*8)+(6*3)+(5*9)+(4*4)+(3*8)+(2*3)+(1*6)=171
171 % 10 = 1
So 83948-36-1 is a valid CAS Registry Number.

83948-36-1Downstream Products

83948-36-1Relevant academic research and scientific papers

Preparation of Primary Amines and 2-Azetidinones via N-Trimethylsilyl Imines

Hart, David J.,Kanai, Ken-ichi,Thomas, Dudley G.,Yang, Teng-Kuei

, p. 289 - 294 (2007/10/02)

Nonenolizable aldehydes react with lithium bis(trimethylsilyl)amide at ambient temperatures to afford solutions of N-trimethylsilyl aldimines.Treatment of these solutions with Grignard reagents or alkyllithiums followed by an aqueous workup gives primary amines in moderate to excellent yields.Treatment of N-trimethylsilyl aldimines with ester enolates provides an expedient route to 1-unsubstituted 2-azetidinones.

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