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111492-68-3

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111492-68-3 Usage

General Description

3-Hydroxy-1-(phenylmethyl)-2-piperidinone, also known as 3-PPP, is a psychoactive research chemical and a derivative of the well-known hallucinogenic drug MPPP. It has been used in scientific research to study its effects on the central nervous system, particularly its interactions with neurotransmitter receptors. 3-PPP acts as a potent dopamine reuptake inhibitor and has been found to have similar effects to other drugs such as Methylphenidate and Cocaine. Due to its psychoactive properties, 3-PPP has potential for abuse and has been regulated in some countries. It is important to handle this chemical with caution and follow safety guidelines when working with it in a laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 111492-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,9 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 111492-68:
(8*1)+(7*1)+(6*1)+(5*4)+(4*9)+(3*2)+(2*6)+(1*8)=103
103 % 10 = 3
So 111492-68-3 is a valid CAS Registry Number.

111492-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Benzyl-3-hydroxypiperidin-2-one

1.2 Other means of identification

Product number -
Other names 3-hydroxy-1-benzyl-2-piperidinone

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:111492-68-3 SDS

111492-68-3Relevant articles and documents

Electrochemical deamination of alkoxyamine lactams

Romero-Iba?ez, Julio,Cruz-Gregorio, Enrique,Cruz-Gregorio, Silvano,Quintero, Leticia,Bernès, Sylvain,González-Perea, Mario,Sartillo-Piscil, Fernando

, (2020)

An anodic electrochemical deamination of 3-alkoxyamine lactams to 3-hydroxy lactams was developed. The electrochemical transformation was achieved by using reticulated vitreous carbon (RVC) and stainless-steel electrodes in aqueous ethanolic solution of NaOAc. This simple electrochemical procedure represents an ecofriendly alternative to the traditional chemical reductive deamination, which requires of a large excess of Zn (up to 40 equivalents) and acetic acid.

Chemoenzymatic enantioselective synthesis of 3-hydroxy-2-pyrrolidinones and 3-hydroxy-2-piperidinones

Kamal, Ahmed,Ramana, K. Venkata,Ramana, A. Venkata,Babu, A. Hari

, p. 2587 - 2594 (2007/10/03)

The enantioselective synthesis of 3-hydroxypyrrolidin-2-ones and 3-hydroxy piperidin-2-ones has been carried out in high enantiomeric excess employing immobilized lipase from Pseudomonas cepacia.

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