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2,5-Diphenyl-4-(1-piperidinylmethylene)-2H-pyrazol-3(4H)-one is a complex organic compound with the molecular formula C23H22N2O. It is a derivative of pyrazolone, a heterocyclic compound with a pyrazole ring fused to a ketone. This specific compound features two phenyl groups at the 2 and 5 positions, a piperidinyl group at the 4 position, and a methylene bridge connecting the piperidinyl group to the pyrazolone core. It is known for its potential applications in medicinal chemistry, particularly as a precursor in the synthesis of various biologically active molecules. The compound's structure and properties make it a subject of interest for researchers exploring new drug candidates and chemical entities with potential therapeutic benefits.

5272-54-8

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5272-54-8 Usage

Molecular structure

2,5-Diphenyl-4-(1-piperidinylmethylene)-2H-pyrazol-3(4H)-one has a complex molecular structure, which includes two phenyl groups and a piperidinylmethylene group.

Pyrazolone derivative

2,5-Diphenyl-4-(1-piperidinylmethylene)-2H-pyrazol-3(4H)-one is a derivative of pyrazolone, a class of organic compounds that are often used in the development of pharmaceutical drugs.

Biological and pharmacological activities

2,5-Diphenyl-4-(1-piperidinylmethylene)-2H-pyrazol-3(4H)-one has potential biological and pharmacological activities, which means it may have effects on living organisms and their physiological functions.

Pharmaceutical drug development

Due to its potential activities, 2,5-Diphenyl-4-(1-piperidinylmethylene)-2H-pyrazol-3(4H)-one may be used in the development of pharmaceutical drugs for various medical conditions.

Interactions with biological receptors or enzymes

The presence of the piperidinylmethylene group suggests that 2,5-Diphenyl-4-(1-piperidinylmethylene)-2H-pyrazol-3(4H)-one may have interactions with biological receptors or enzymes, making it a potential target for drug development.

Need for further research

To fully understand the properties and potential applications of 2,5-Diphenyl-4-(1-piperidinylmethylene)-2H-pyrazol-3(4H)-one, further research and investigation are needed. This includes studying its interactions with biological systems, potential therapeutic effects, and possible side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 5272-54-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,7 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5272-54:
(6*5)+(5*2)+(4*7)+(3*2)+(2*5)+(1*4)=88
88 % 10 = 8
So 5272-54-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H21N3O/c25-21-19(16-23-14-8-3-9-15-23)20(17-10-4-1-5-11-17)22-24(21)18-12-6-2-7-13-18/h1-2,4-7,10-13,16H,3,8-9,14-15H2/b19-16-

5272-54-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4Z)-2,5-diphenyl-4-(piperidin-1-ylmethylidene)pyrazol-3-one

1.2 Other means of identification

Product number -
Other names 2-Pyrazolin-5-one,1,3-diphenyl-4-(piperidinomethylene)

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:5272-54-8 SDS

5272-54-8Downstream Products

5272-54-8Relevant academic research and scientific papers

Enaminone in heterocyclic synthesis: Synthesis of new pyrazolopyrazole, pyrazolothienooxazine and pyrazolothienopyridine derivatives

Hafiz, Ibrahim Saad Abdel,Reheim, Mohamed Ahmed Mahmoud Abdel,Baker, Safaa Mohamed,Ramiz, Mahmoud Mahfouz

, p. 1133 - 1144 (2015/01/30)

The chemical reactivity of enaminone 2 toward some nucleophilic and electrophilic reagents was investigated. Enaminone 2 was used as a key precursor for the synthesis of many important heterocyclic compounds. The synthesized compounds were characterized b

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