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6219-55-2

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6219-55-2 Usage

General Description

1-(4-Nitrophenyl)-1H-1,2,4-Triazole is a chemical compound with the molecular formula C9H6N4O2. It is a triazole derivative with a 4-nitrophenyl group attached to the triazole ring. 1-(4-Nitrophenyl)-1H-1,2,4-Triazole has various potential applications, including as a building block in the synthesis of pharmaceuticals, agrochemicals, and materials, and as a research tool in the study of biological processes. It has also been investigated for its potential biological activities, including antiviral, antimicrobial, and anticancer properties. However, it is important to handle this compound with care, as it may have hazardous properties and should be used in a controlled environment by trained personnel following proper safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 6219-55-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,1 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6219-55:
(6*6)+(5*2)+(4*1)+(3*9)+(2*5)+(1*5)=92
92 % 10 = 2
So 6219-55-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N4O2/c13-12(14)8-3-1-7(2-4-8)11-6-9-5-10-11/h1-6H

6219-55-2SDS

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)-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names TRI003

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:6219-55-2 SDS

6219-55-2Relevant articles and documents

N-Heterocyclic Carbene Copper(I) Complex Catalyzed Coupling of (Hetero)aryl Chlorides and Nitrogen Heterocycles: Highly Efficient Catalytic System

Zhang, Mengyao,Zhang, Yingying,Zhang, Huixin,Zeng, Yongfei,Liu, Guiyan

, p. 1252 - 1256 (2020/08/05)

A highly efficient catalytic system for the N-arylation reactions of (hetero)aryl chlorides and nitrogen heterocycles with a copper(I) complex containing a 1,10-phenanthroline analogue N-heterocyclic carbene (NHC) has been reported. The complex was characterized by 1H NMR and 13C NMR spectroscopy and elemental analysis, and its structure was determined by single-crystal X-ray diffraction. The NHC-copper(I) complex was employed as pre-catalyst for Ullmann type N-arylation reactions of (hetero)aryl chlorides with various azoles. A variety of hindered and functionalized azoles and (hetero)aryl chlorides were transformed in good to excellent yields.

Copper nanoparticles incorporated on a mesoporous carbon nitride, an excellent catalyst in the Huisgen 1,3-dipolar cycloaddition and N-arylation of N-heterocycles

Kazemi Movahed, Siyavash,Salari, Parinaz,Kasmaei, Melika,Armaghan, Mahsa,Dabiri, Minoo,Amini, Mostafa M.

, (2017/10/06)

Cu nanoparticles with average particles size around 10?nm were incorporated on the surface of a mesoporous carbon nitride support. The XRD and N2 adsorption isotherms show that it maintains a hexagonal mesoporous structure with a high surface a

HEPARAN SULFATE BIOSYNTHESIS INHIBITORS FOR THE TREATMENT OF DISEASES

-

Paragraph 000498, (2016/05/02)

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions in need of inhibition of heparan sulfate biosynthesis.

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