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Pipermethystine, a phenethylamine derivative, is a structural analog of the stimulant drug MDMA (ecstasy). It exhibits similar psychoactive properties and acts as a releasing agent for serotonin, dopamine, and norepinephrine, increasing their levels in the brain. Although it has been studied for potential use in treating depression, anxiety, and as a recreational drug, it is not approved for medical use and is a controlled substance in many countries due to its potential for abuse and addiction. Ongoing research is focused on its safety and efficacy, and caution is advised in its consideration for use.

71627-22-0

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71627-22-0 Usage

Uses

Used in Pharmaceutical Research:
Pipermethystine is used as a research compound for studying its potential therapeutic effects on conditions such as depression and anxiety. Its psychoactive properties and ability to release neurotransmitters like serotonin, dopamine, and norepinephrine make it a subject of interest in the field of psychopharmacology.
Used in Recreational Drug Use:
Despite its lack of medical approval, pipermethystine is used as a recreational drug due to its psychoactive effects. However, its potential for abuse and addiction has led to its classification as a controlled substance in many countries.

Check Digit Verification of cas no

The CAS Registry Mumber 71627-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,2 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71627-22:
(7*7)+(6*1)+(5*6)+(4*2)+(3*7)+(2*2)+(1*2)=120
120 % 10 = 0
So 71627-22-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H17NO4/c1-12(18)21-14-8-10-16(20)17(11-14)15(19)9-7-13-5-3-2-4-6-13/h2-6,8,10,14H,7,9,11H2,1H3

71627-22-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [6-oxo-1-(3-phenylpropanoyl)-2,3-dihydropyridin-3-yl] acetate

1.2 Other means of identification

Product number -
Other names (+/-)-5-acetoxy-5,6-dihydro-N-(1-oxo-3-phenylpropyl)-2(1H)-pyridone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:71627-22-0 SDS

71627-22-0Downstream Products

71627-22-0Relevant academic research and scientific papers

Facile enantiodivergent approach to 5-hydroxy-5,6-dihydro-2(1H)-pyridones. First total synthesis of both enantiomers of pipermethystine.

Arrayas,Alcudia,Liebeskind

, p. 3381 - 3383 (2007/10/03)

[reaction: see text]. A novel enantiodivergent approach to 5-hydroxy-5,6-dihydro-2(1H)-pyridones using a ring closing metathesis and a lipase-mediated kinetic resolution as key steps is described and applied to the first synthesis of both enantiomers of pipermethystine.

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