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28058-13-1 Usage

Molecular Structure

2-[2-(4-chlorobenzylidene)hydrazinyl]-5-nitropyridine consists of a nitropyridine ring with a 4-chlorobenzylidene hydrazinyl group as a substituent.

Usage

It is used as a precursor in the synthesis of other organic compounds and pharmaceutical intermediates.

Potential Applications

It has potential applications in the development of new drugs, such as anti-cancer and anti-inflammatory agents.

Value in Research

Its chemical properties and reactivity make it a valuable building block in organic synthesis and drug discovery research.

Other Possible Uses

It may also have uses in the field of materials science and organic electronics.

Check Digit Verification of cas no

The CAS Registry Mumber 28058-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,5 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28058-13:
(7*2)+(6*8)+(5*0)+(4*5)+(3*8)+(2*1)+(1*3)=111
111 % 10 = 1
So 28058-13-1 is a valid CAS Registry Number.

28058-13-1SDS

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	N-[(4-chlorophenyl)methylideneamino]-5-nitropyridin-2-amine

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:28058-13-1 SDS

28058-13-1Upstream product

28058-13-1Downstream Products

28058-13-1Relevant academic research and scientific papers

Chemotherapeutically effective nitro compounds. III. Nitropyridines, nitroimidazopyridines and related compounds

Winkelmann,Raether,Hartung,Wagner

, p. 82 - 89 (2007/10/04)

New 2 nitropyridines and 3 nitropyridines, and 3 nitroimidazo [1,2 a] pyridines and related compounds (together 106) were synthesized and tested for their chemotherapeutic efficacy against trichomonads, amoebas and other organisms, such as Eimeria tenella, bacteria, fungi and helminths. Several 2 nitropyridines revealed a detectable systemic effect against Entamoeba histolytica (extraintestinal amoebiasis of the golden hamster) and also a weak activity against Trichomonas fetus in the NMRI mouse. Only a few 3 nitropyridines showed a marked systemic effect against trichomonads. Of the 3 nitroimidazo [1,2 a] pyridines, only the electroneutral carboxylic acid amide group exhibited a pronounced activity, exclusively against trichomonads; however, the activity was nullified by electronegative, electropositive and other electroneutral substituents. As they were not superior in chemotherapeutic respect compared to the known standard preparations (metronidazole), no further tests were carried out with the most effective compounds.

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28058-13-1

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