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110231-11-3

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110231-11-3 Usage

Chemical class

Piperazine derivatives

Salt form

Hydrochloride

Common use

Pharmaceutical research as a potential antipsychotic agent

Molecular structure

Piperazine ring attached to a pyrrolidinone ring

Psychoactive properties

Due to the presence of the piperazine and pyrrolidinone rings

Additional studies

Potential use in treating neurological disorders and mood-related conditions

Safety precautions

Handle and use with caution due to significant effects on the central nervous system and other biological functions

Check Digit Verification of cas no

The CAS Registry Mumber 110231-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,2,3 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110231-11:
(8*1)+(7*1)+(6*0)+(5*2)+(4*3)+(3*1)+(2*1)+(1*1)=43
43 % 10 = 3
So 110231-11-3 is a valid CAS Registry Number.

110231-11-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(4-benzhydrylpiperazin-1-yl)-2-oxoethyl]pyrrolidin-2-one,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:110231-11-3 SDS

110231-11-3Downstream Products

110231-11-3Relevant articles and documents

Pyrrolidone and piperidone derivatives with antihistaminic and antianaphylactic activities. Synthesis and pharmacological study

de Meglio,Corradi,Ravenna,Gentili,Tempra-Gabbiati,Cristina,Riva

, p. 359 - 382 (2007/10/02)

The preparation of several derivatives to oxatomide (A), with the benzimidazolinone moiety replaced by another heterocyclic residue is described. In some cases changes to the basic chain of (A) were also considered. All the new compounds were evaluated as

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