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3,3-diphenyl-1-(piperazin-1-yl)propan-1-one is a chemical compound with the molecular formula C19H22N2O. It is a ketone derivative that contains a piperazine group, which is a six-membered heterocyclic ring with two nitrogen atoms. 3,3-diphenyl-1-(piperazin-1-yl)propan-1-one is commonly used as a building block for the synthesis of pharmaceuticals and other organic compounds.

88372-34-3

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88372-34-3 Usage

Uses

Used in Pharmaceutical Industry:
3,3-diphenyl-1-(piperazin-1-yl)propan-1-one is used as a building block for the synthesis of pharmaceuticals for its potential pharmacological activities, particularly as an analgesic and anesthetic agent.
Used in Chemical Industry:
3,3-diphenyl-1-(piperazin-1-yl)propan-1-one is used as a precursor in the synthesis of novel drugs and chemical compounds, contributing to the development of new organic compounds with various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 88372-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,7 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88372-34:
(7*8)+(6*8)+(5*3)+(4*7)+(3*2)+(2*3)+(1*4)=163
163 % 10 = 3
So 88372-34-3 is a valid CAS Registry Number.

88372-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-diphenyl-1-piperazin-1-ylpropan-1-one

1.2 Other means of identification

Product number -
Other names 3,3-diphenyl-1-piperazin-1-yl-propan-1-one

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:88372-34-3 SDS

88372-34-3Relevant academic research and scientific papers

Substituted piperizines for the treatment of pain

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Page/Page column 7, (2008/12/06)

The present invention is directed to the use of substituted piperizine compounds represented by Formula I, for the treatment of pain, including acute pain, chronic pain, cancer pain, visceral pain, inflammatory pain, neuropathic pain, post-herpetic neural

ISOXAZOLE DERIVATIVES AS CALCIUM CHANNEL BLOCKERS

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Page/Page column 30, (2008/06/13)

Methods and compounds effective in ameliorating conditions characterized by unwanted calcium channel activity, particularly unwanted N-type or T-type calcium channel activity are disclosed. Specifically, a series of isoxazole containing compounds are disclosed of the general formula (1) where Z is N or CHNR3 and (Ar1)2CR4 is optionally substituted benzhydryl.

Preferentially substituted calcium channel blockers

-

, (2008/06/13)

Certain piperazine substituted compounds are described which are useful in altering calcium channel activity.

(Pyridylcyanomethyl)piperazines as orally active PAF antagonists

Carceller,Almansa,Merlos,Giral,Bartroli,Garcia-Rafanell,Forn

, p. 4118 - 4134 (2007/10/02)

A series of (pyridylcyanomethyl)piperazines was prepared and evaluated for PAF-antagonist activity. Compounds were tested in vitro in a PAF-induced platelet aggregation assay and in vivo in a PAF-induced hypotension test in normotensive rats. Oral activity was ascertained through a PAF-induced mortality test in mice. The main structure-activity trends of the series were established. Activity was mainly found in four skeletons: 1-acyl-4-(3- pyridylcyanomethyl)-piperazine, 1-acyl-4-(4-pyridylcyanomethyl)piperazine, 1- acyl-4-(3-pyridylcyanomethyl)piperidine, and 1-acyl-4-cyano-4-(3- pyridylamino)piperidine. The acyl substituents, diphenylacetyl and 3,3- diphenylpropionyl, provided the most active compounds, and the introduction of an amine or hydroxy group in the 3,3-diphenylpropionyl substituent led to further improvement in oral activity. As a result, three of the most active compounds (100, 114, and 115) have been selected for further pharmacological development.

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