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1H-Pyrazole, 5-(3-chlorophenyl)-4,5-dihydro-1,3-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57488-03-6

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57488-03-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57488-03-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,8 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 57488-03:
(7*5)+(6*7)+(5*4)+(4*8)+(3*8)+(2*0)+(1*3)=156
156 % 10 = 6
So 57488-03-6 is a valid CAS Registry Number.

57488-03-6SDS

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 3-(3-chlorophenyl)-2,5-diphenyl-3,4-dihydropyrazole

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:57488-03-6 SDS

57488-03-6Relevant academic research and scientific papers

Spectroscopic studies of aryl substituted 1-phenyl-2-pyrazolines: Steric and electronic substitution effects

Soltani, Marzieh,Memarian, Hamid R.,Sabzyan, Hassan

, p. 903 - 917 (2018/09/18)

A series of aryl substituted 1-phenyl-2-pyrazolines containing electron-donating and electron-withdrawing substituents on different positions of the C3– or C5-aryl groups were synthesized and their steric and electronic effects on ch

Ultrasound assisted synthesis of 1,5-diaryl and 1,3,5-triaryl-2-pyrazolines by using KOH/EtOH system with Cu(I) catalyst

Pise, Ashok S.,Jadhav, Sunil D.,Burungale, Arvind S.,Devkate, Santosh S.,Gawade, Ramesh B.

, p. 894 - 896 (2018/03/13)

1,5-Diaryl-2-pyrazolines and 1,3,5-triaryl-2-pyrazolines were synthesized in alcoholic potassium hydroxide in high yields within 1-6 min under ultrasound irradiation at room temperature.

Nanocasting, Template Synthesis, and Structural Studies on Cesium Salt of Phosphotungstic Acid for the Synthesis of Novel 1,3,5-Triaryl-pyrazoline Derivatives

Fazaeli, Razieh,Aliyan, Hamid,Tangestaninejad, Shahram,Mohammadi, Esmaeel,Bordbar, Maryam

, p. 237 - 246 (2016/04/19)

The elimination of the silica matrix of composites by HF occurred by a two-step reaction deposition of a Cs2.5H0.5PW12O40 (CsHPW) salt nanocrystal. We used 2D hexagonal SBA-15 silica as a template for the nanofabrication of CsHPW nanoparticles. Nanocast CsHPW materials are stable against leaching and colloidization in polar solvents. The catalytic performance of the nanocast CsHPW materials exceeded that of bulk Cs2.5H0.5PW12O40, which is the most active among the acidic HPW salts. A series of novel 1,3,5-triaryl-pyrazoline derivatives were synthesized by the reaction between chalcone and phenylhydrazine in high yield in the presence of CsHPW salt nanocrystals.

A convenient and efficient protocol for the synthesis of 1,3,5-triaryl-2-pyrazolines in acetic acid under ultrasound irradiation

Lin, Zhi-Ping,Li, Ji-Tai

experimental part, p. 267 - 271 (2012/06/18)

1,3,5-Triaryl-2-pyrazolines were synthesized in acetic acid in high yields within 60-180 min under ultrasound irradiation at room temperature.

Nanocasting, template synthesis, and structural studies on cesium salt of phosphotungstic acid for the synthesis of novel 1,3,5-triaryl-pyrazoline derivatives

Fazaeli, Razieh,Aliyan, Hamid,Tangestaninejad, Shahram,Mohammadi, Esmaeel,Bordbar, Maryam

experimental part, p. 237 - 246 (2012/06/30)

The elimination of the silica matrix of composites by HF occurred by a two-step reaction deposition of a Cs2.5H0.5PW 12O40 (CsHPW) salt nanocrystal. We used 2D hexagonal SBA-15 silica as a template for the nanof

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