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

62160-33-2

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62160-33-2 Usage

Structure

Pyrazole derivative with a nitrophenyl and phenyl group attached to the nitrogen atom

Usage

Commonly used in organic synthesis and pharmaceutical research, exhibits a range of biological activities

Applications

Useful for the development of various pharmaceuticals and agrochemicals

Versatility

Used as a building block for the synthesis of other organic compounds, due to its reactivity and versatility.

Check Digit Verification of cas no

The CAS Registry Mumber 62160-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,6 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62160-33:
(7*6)+(6*2)+(5*1)+(4*6)+(3*0)+(2*3)+(1*3)=92
92 % 10 = 2
So 62160-33-2 is a valid CAS Registry Number.

62160-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-nitrophenyl)-5-phenylpyrazole

1.2 Other means of identification

Product number -
Other names 1-<4-Nitro-phenyl>-5-phenyl-pyrazol

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:62160-33-2 SDS

62160-33-2Downstream Products

62160-33-2Relevant academic research and scientific papers

Copper-mediated tandem ring-opening/cyclization reactions of cyclopropanols with aryldiazonium salts: Synthesis of: N -arylpyrazoles

Liu, Jidan,Xu, Erjie,Jiang, Jinyuan,Huang, Zeng,Zheng, Liyao,Liu, Zhao-Qing

supporting information, p. 2202 - 2205 (2020/02/26)

A general method for the synthesis of structurally diverse N-arylpyrazoles from readily available cyclopropanols and aryldiazonium salts is disclosed. The reaction was conducted at room temperature within minutes with a broad substrate scope and excellent regioselectivity.

Regioselective microwave-assisted synthesis of substituted pyrazoles from ethynyl ketones

Bagley, Mark C.,Lubinu, M. Caterina,Mason, Christopher

, p. 704 - 708 (2007/12/27)

Reaction of α,β-ethynyl ketones and hydrazine derivatives gives 1,3- and 1,5-disubstituted pyrazoles in good yield. Microwave irradiation in concentrated hydrochloric acid-methanol (1.5% v/v), with concurrent cooling at sub-ambient temperatures or at 120°

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