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3,5-bis(4-fluorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazole is a complex organic compound with the molecular formula C20H15F2N2. It is characterized by a pyrazole ring, which is a five-membered heterocyclic ring containing two nitrogen atoms. The molecule features two 4-fluorophenyl groups attached to the 3 and 5 positions of the pyrazole ring, and a phenyl group attached to the 1 position. 3,5-bis(4-fluorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazole is a derivative of pyrazole and is known for its potential applications in pharmaceuticals and materials science due to its unique structure and properties. It is synthesized through various chemical reactions and can be used as a building block for the development of new drugs or as a ligand in coordination chemistry.

5304-07-4

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5304-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5304-07-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,0 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5304-07:
(6*5)+(5*3)+(4*0)+(3*4)+(2*0)+(1*7)=64
64 % 10 = 4
So 5304-07-4 is a valid CAS Registry Number.

5304-07-4SDS

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 3,5-bis(4-fluorophenyl)-1-phenyl-4,5-dihydro-1H-pyrazole

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

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More Details:5304-07-4 SDS

5304-07-4Downstream Products

5304-07-4Relevant academic research and scientific papers

Synthesis and anticancer activity of 1,3,5-triaryl-1H-pyrazole

Ghadbeigi, Sajad,Ostad, Seyed Nasser,Shafiee, Abbas,Amini, Mohsen

, p. 754 - 759 (2015/10/05)

Previous studies demonstrated that some pyrazole derivatives could be considered as potential anticancer agents. A series of 1,3,5-triaryl-1H-pyrazole derivatives were prepared by the reaction of phenylhydrazin and different chalcones. The previous classi

Antimicrobial, analgesic, DPPH scavenging activities and molecular docking study of some 1,3,5-triaryl-2-pyrazolines

Samshuddin, Seranthimata,Narayana, Badiadka,Sarojini, Balladka Kunhanna,Raj, Chenna Govindaraju Darshan,Khan, Mahmud Tareq Hassan,Yathirajan, Hemmige S.,Raghavendra, Ramappa

, p. 2012 - 2022,11 (2020/07/30)

A series of 1,3,5-triaryl-2-pyrazolines 2a-g were synthesized by the reaction of 4,40-disubstituted chalcone with phenyl hydrazine. All these compounds were characterized by NMR, IR and mass spectral and single crystal XRD data. All the synthesized produc

New 2-pyrazolines of anticipated molluscicidal activity

Mishriky,Asaad,Ibrahim,Girgis

, p. 544 - 548 (2007/10/03)

A facile one-pot synthesis of 1-substituted carbamoyl or thiocarbamoyl-2-pyrazolines 6 is described. Also, the synthesis as well as the molluscicidal activity of 1,3,5-triaryl- (2), 1-acetyl-3,5-diaryl- (4) 2-pyrazolines are outlined.

New 2-pyrazolines of anticipated molluscicidal activity

Mishriky, Nawal,Asaad, Fahmy M.,Ibrahim, Yehia A.,Girgis, Adel S.

, p. 935 - 940 (2007/10/03)

A facile one-pot synthesis of 1-substituted carbamoyl- or thiocarbamoyl-2-pyrazolines 6 is described. The synthesis as well as molluscicidal activity of 1,3,5-triaryl- and 1-acetyl-3,5-diaryl-2-pyrazolines (2 and 4) are also outlined.

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