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5-(3-nitrophenyl)-1,3-diphenyl-4,5-dihydro-1H-pyrazole is a complex organic compound with the molecular formula C20H16N3O2. It is a derivative of pyrazole, a five-membered heterocyclic ring containing two nitrogen atoms. The compound features a 3-nitrophenyl group attached to the 5-position of the pyrazole ring, and two phenyl groups attached to the 1 and 3 positions. The presence of the nitro group (-NO2) on the phenyl ring imparts unique chemical and physical properties to the molecule. 5-(3-nitrophenyl)-1,3-diphenyl-4,5-dihydro-1H-pyrazole is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its structural diversity and reactivity.

6969-04-6

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6969-04-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6969-04-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6969-04:
(6*6)+(5*9)+(4*6)+(3*9)+(2*0)+(1*4)=136
136 % 10 = 6
So 6969-04-6 is a valid CAS Registry Number.

6969-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-nitrophenyl)-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

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More Details:6969-04-6 SDS

6969-04-6Relevant articles and documents

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.

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

Mechanically activated synthesis of 1,3,5-triaryl-2-pyrazolines by high speed ball milling

Zhu, Xingyi,Li, Zhenhua,Jin, Can,Xu, Li,Wu, Qianqian,Su, Weike

experimental part, p. 163 - 165 (2010/04/22)

An efficient mechanically activated solvent-free synthesis of 1,3,5-triaryl-2-pyrazolines from chalcones and phenylhydrazines using high speed ball milling is described. This method has notable advantages in terms of good yield, short reaction time and ne

Synthesis of some new bioactive 1-N-subtituted 3,5-diaryl-2-pyrazolines

Khan, Sadaf Sadiq,Hasan, Aurangzeb

, p. 131 - 138 (2008/02/12)

A group of four series (A-D) of 22 new bioactive 1-N-acid substituted 3, 5-diphenyl-2-pyrazolines were synthesized by cyclization of variably substituted chalcones and simple or substituted phenyl hydrazine and / or semicarbazide, using acetic acid as a s

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