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3-amino-1-phenyl-4,5-dihydropyrazolin-5-one is an organic compound characterized by the presence of an amino group, a phenyl group, and a dihydropyrazolin-5-one ring structure. It is recognized for its potential as a building block in the synthesis of pharmaceuticals and agrochemicals, as well as for its analgesic and anti-inflammatory properties, which position it as a promising candidate for the development of new drugs for pain management and inflammatory conditions. Its unique structure also contributes to its value as an intermediate in the synthesis of other complex organic molecules and in the creation of fluorescent probes for biological imaging.

28710-97-6

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28710-97-6 Usage

Uses

Used in Pharmaceutical Industry:
3-amino-1-phenyl-4,5-dihydropyrazolin-5-one is used as a building block for the synthesis of various pharmaceuticals due to its versatile chemical structure, which allows for the development of new drugs with analgesic and anti-inflammatory properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-amino-1-phenyl-4,5-dihydropyrazolin-5-one serves as a key intermediate in the synthesis of agrochemicals, contributing to the development of effective products for agricultural applications.
Used in Medicinal Chemistry:
3-amino-1-phenyl-4,5-dihydropyrazolin-5-one is utilized as a valuable intermediate in the synthesis of complex organic molecules, facilitating advancements in medicinal chemistry through the creation of novel compounds with potential therapeutic applications.
Used in Chemical Biology:
3-amino-1-phenyl-4,5-dihydropyrazolin-5-one is employed in the development of fluorescent probes for biological imaging applications, enhancing the study of biological processes and contributing to chemical biology research.
Overall, 3-amino-1-phenyl-4,5-dihydropyrazolin-5-one is a multifaceted chemical with a broad spectrum of applications, particularly in the fields of medicinal chemistry and chemical biology, where its unique attributes are leveraged to innovate and improve upon existing methodologies and compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 28710-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,7,1 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28710-97:
(7*2)+(6*8)+(5*7)+(4*1)+(3*0)+(2*9)+(1*7)=126
126 % 10 = 6
So 28710-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9N3O/c10-8-6-9(13)12(11-8)7-4-2-1-3-5-7/h1-6,11H,10H2

28710-97-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-2-phenyl-1H-pyrazol-3-one

1.2 Other means of identification

Product number -
Other names 5-amino-2-phenyl-1,2-dihydropyrazol-3-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:28710-97-6 SDS

28710-97-6Relevant academic research and scientific papers

Synthesis, characterization and biological activity of some pyrazole-pyrazolone derivatives

Sayed,Negm,Azab,Anwer

, p. 663 - 672 (2017/04/13)

SIX heterocyclic compounds were synthesized based on pyrazole and pyrazolone rings. The chemical structures of the synthesized compounds were characterized by using: elemental analysis, FTIR, 1H-NMR, 13C-NMR and Mass spectra. The compounds were evaluated for their activity against gram +ve, gram -ve bacteria and fungi. The antimicrobial assessment showed the high activity of compounds I and VI.

Synthesis, characterization and biological activity of some pyrazole-pyrazolone derivatives

Sayed,Negm,Azab,Anwer

, p. 663 - 672 (2017/04/17)

SIX heterocyclic compounds were synthesized based on pyrazole and pyrazolone rings. The chemical structures of the synthesized compounds were characterized by using: elemental analysis, FTIR, 1H-NMR, 13C-NMR and Mass spectra. The compounds were evaluated for their activity against gram +ve, gram-ve bacteria and fungi. The antimicrobial assessment showed the high activity of compounds I and VI.

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