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

5920-39-8

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5920-39-8 Usage

Class

pyrazole derivatives

Structural features

comprised of a pyrazole ring substituted with a 4,5-dihydro-1-(4-nitrophenyl)-3-phenyl group

Usage

commonly used in the synthesis of various pharmaceuticals and agrochemicals

Biological activities

studied for its potential anticancer, antifungal, and antimicrobial properties

Value

valuable building block for the development of new drugs and agricultural products, and a valuable candidate for further research in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 5920-39-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,2 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5920-39:
(6*5)+(5*9)+(4*2)+(3*0)+(2*3)+(1*9)=98
98 % 10 = 8
So 5920-39-8 is a valid CAS Registry Number.

5920-39-8SDS

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 2-(4-nitrophenyl)-5-phenyl-3,4-dihydropyrazole

1.2 Other means of identification

Product number -
Other names 1H-Pyrazole,4,5-dihydro-1-(4-nitrophenyl)-3-phenyl

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:5920-39-8 SDS

5920-39-8Relevant academic research and scientific papers

Divergent Synthesis of 1H-Indazoles and 1H-Pyrazoles from Hydrazones via Iodine-Mediated Intramolecular Aryl and sp3 C–H Amination

Wei, Wei,Wang, Zhen,Yang, Xikang,Yu, Wenquan,Chang, Junbiao

, p. 3378 - 3387 (2017/10/09)

A divergent intramolecular C–H amination of hydrazones has been developed employing molecular iodine (I2) as the sole oxidant. The required hydrazone substrates were readily obtained by condensation of hydrazines with the corresponding ketones.

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