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1-(4-FLUOROPHENYL)-3-HYDROXY-4,5-DIHYDRO-1H-PYRAZOLE is a pyrazole derivative chemical compound with the molecular formula C9H9FN2O. It features a 1-(4-fluorophenyl) group attached to a 3-hydroxy-4,5-dihydro-1H-pyrazole ring, which endows it with potential pharmacological properties. 1-(4-FLUOROPHENYL)-3-HYDROXY-4,5-DIHYDRO-1H-PYRAZOLE is of interest in the fields of medicinal and pharmaceutical research due to its unique structure and possible applications.

6119-11-5

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6119-11-5 Usage

Uses

Used in Pharmaceutical Research:
1-(4-FLUOROPHENYL)-3-HYDROXY-4,5-DIHYDRO-1H-PYRAZOLE is used as a chemical intermediate for the development of new pharmaceuticals. Its unique structure allows for the potential creation of novel drugs with improved efficacy and reduced side effects.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(4-FLUOROPHENYL)-3-HYDROXY-4,5-DIHYDRO-1H-PYRAZOLE is used as a building block for designing and synthesizing new molecules with therapeutic potential. Its incorporation into various molecular frameworks can lead to the discovery of new drugs for treating a wide range of diseases.
Used in Drug Delivery Systems:
1-(4-FLUOROPHENYL)-3-HYDROXY-4,5-DIHYDRO-1H-PYRAZOLE can be utilized in the development of drug delivery systems, where its chemical properties may enhance the solubility, stability, or targeted delivery of therapeutic agents. This application can improve the bioavailability and overall effectiveness of drugs in the treatment of various medical conditions.
Used in Chemical Synthesis:
As a pyrazole derivative, 1-(4-FLUOROPHENYL)-3-HYDROXY-4,5-DIHYDRO-1H-PYRAZOLE can be employed in chemical synthesis processes to create a variety of new compounds with diverse applications, including those in the fields of materials science, agrochemistry, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 6119-11-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,1 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6119-11:
(6*6)+(5*1)+(4*1)+(3*9)+(2*1)+(1*1)=75
75 % 10 = 5
So 6119-11-5 is a valid CAS Registry Number.

6119-11-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-fluorophenyl)pyrazolidin-3-one

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:6119-11-5 SDS

6119-11-5Downstream Products

6119-11-5Relevant academic research and scientific papers

Ring-closing metathesis as a key step to construct the 2, 6-dihydropyrano[2, 3-c]pyrazole ring system

Bieliauskas, Aurimas,Krik?tolaityte, Sonata,Holzer, Wolfgang,?ackus, Algirdas

, p. 296 - 307 (2018/09/10)

A simple and efficient synthetic route to the 2, 6-dihydropyrano[2, 3-c]pyrazole ring system was developed by employing ring-closing metathesis (RCM) as a key step. The required diene substrate for the RCM reaction was prepared by a three-step procedure s

A convenient one-pot synthesis of 1-aryl-substituted 4-iodopyrazol-3-ols via aromatisation and oxidative iodination reactions

Liu, Jingjing,Yang, Shanguang,Dong, Ruimei,Jin, Zhudan,Wang, Mingliang

, p. 24 - 27 (2018/02/28)

A convenient and economical one-pot synthesis of a series of new 1-aryl-substituted 4-iodopyrazole-3-ols from easily available pyrazolidin- 3-ones in the presence of sodium iodide, 30% solution of hydrogen peroxide and a catalytic amount of sulfuric acid in dichloromethane via aromatisation and oxidative iodination reactions are described. This protocol has the advantages of high atom economy, costeffectiveness, short reaction time and environmental friendliness.

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