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(6Z)-2,4-dichloro-6-[(2-hydroxy-1,1-dimethylethyl)amino]methylidenecyclohexa-2,4-dien-1-one, commonly known as Chlorfenapyr, is an insecticide and acaricide belonging to the pyrrole and halogenated aromatic compound class. It is characterized by its ability to control a broad spectrum of pests on various crops, such as vegetables, fruits, and cotton. Chlorfenapyr operates by disrupting the metabolic processes of insects and mites, ultimately leading to their death. It is recognized for its effectiveness against insecticide-resistant pests, making it a valuable tool in agricultural pest management. However, it is crucial to exercise caution when handling and applying Chlorfenapyr due to its potential toxicity to non-target organisms and possible harmful effects on human health if not used correctly.

4936-83-8

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4936-83-8 Usage

Uses

Used in Agricultural Industry:
Chlorfenapyr is used as an insecticide and acaricide for controlling a wide range of pests on various crops, including vegetables, fruits, and cotton. Its application is aimed at protecting these crops from damage caused by insects and mites, ensuring a healthy and productive yield.
Used in Pest Management:
Chlorfenapyr serves as a valuable tool in pest management due to its broad-spectrum activity and effectiveness against insecticide-resistant pests. It is particularly useful in situations where traditional insecticides have proven ineffective, providing an alternative solution to combat resistant pest populations.
Used in Integrated Pest Management (IPM) Programs:
Chlorfenapyr can be incorporated into Integrated Pest Management (IPM) programs, which aim to minimize the use of chemical pesticides and promote environmentally friendly pest control methods. By using Chlorfenapyr in combination with other pest control strategies, such as biological control, cultural practices, and monitoring, it is possible to achieve more sustainable and effective pest management.

Check Digit Verification of cas no

The CAS Registry Mumber 4936-83-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,3 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4936-83:
(6*4)+(5*9)+(4*3)+(3*6)+(2*8)+(1*3)=118
118 % 10 = 8
So 4936-83-8 is a valid CAS Registry Number.

4936-83-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (6Z)-2,4-dichloro-6-[[(1-hydroxy-2-methylpropan-2-yl)amino]methylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names (E)-2,4-dichloro-6-((1-hydroxy-2-methylpropan-2-ylimino)methyl)phenol

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:4936-83-8 SDS

4936-83-8Downstream Products

4936-83-8Relevant academic research and scientific papers

A mechanistic approach for in-vitro anticancer activity via nucleic acid fragmentation by copper(II) complex anchored on MCM-41

Biswas, Subhendu,Das, Debasis,Dasgupta, Sanchari,Karim, Suhana,Parveen, Rumana

, (2022/01/11)

Three new mononuclear copper Schiff base complexes, namely, ([Cu(L1)Cl].CH3CN (HmC_1), [Cu(L2)Cl].CH3CN (HmC_2) and [Cu(L3)Cl].CH3CN (HmC_3) derived from ONO donor tridentate ligands HL1, HL2 and HL3, respectively, have been synthesized to check their efficacy as target-specific next-generation anticancer therapeutics. All the HmCs have been characterized by using various physicochemical techniques (i.e., single-crystal X-ray analysis, Fourier transform infrared [FT-IR] spectroscopy and elemental analysis). Among the synthesized Schiff base complexes, HmC_3 was turned out to be most effective in killing cancer cell carried out on cultured human breast cancer cell line (MDA-MB-231) and human lung carcinoma cell line (A549). Finally, in order to improve the cellular permeability, particle size of HmC_3 was scaling down to nano-regime by immobilizing it onto a suitable matrix MCM-41@APTES (MCM-41 = Mobil Composition of Matter No. 41 and APTES = 3-aminopropyltriethoxysilane) to generate MCM-41@APTES@HmC_3 (MCM-41@APTES@HmC_3 = HtC_3). Field-emission scanning electron microscope (FESEM) and dynamic light scattering (DLS) study revealed the particle size of the synthesized HtC_3 nano-composite was within nano-regime and therefore could be further effective for biomedical applications. Furthermore, HtC_3 displayed better cancer cell killing property. To get insight into the mechanism of action of HtC_3, Annexin V-FITC/PI analysis and TUNEL assay revealed that DNA damage phenomenon is accompanied with changes in cellular morphology leading to cell apoptosis. Cell migration assay on MDA-MB-231 cell with HtC_3 exposed the effectiveness of HtC_3 in arresting cancer cell migration. Therefore, all the in-vitro studies demonstrated that the immobilization of the copper Schiff base complex onto a suitable matrix increased its efficiency and becomes a promising anticancer nano-therapeutic agent.

A Schiff base zinc compound, preparation method thereof and method for producing polylactic acid

-

Paragraph 0101; 0102; 0104, (2017/10/27)

The invention provides a schiff base zinc compound which is in a structure as shown in Formula 1, wherein R1 and R2 are independently selected from -H, alkyl, halogen and -NO2; R3, R4 and R5 are independently selected from -H and -CH3; R' is alkoxyl or -O

A Schiff base aluminum compound, preparation method thereof and method for producing polylactic acid

-

Paragraph 0111; 0112; 0113; 0114, (2017/08/25)

The invention provides a Schiff base aluminum compound and a preparation method thereof, and a polylactic acid preparation method. The Schiff base aluminum compound provided by the invention has a structure shown in Formula (I) or Formula (II), wherein R1

Racemization of secondary alcohols catalyzed by ruthenium: Application to chemoenzymatic dynamic resolution

Merabet-Khelassi, Mounia,Vriamont, Nicolas,Aribi-Zouioueche, Louisa,Riant, Olivier

experimental part, p. 1790 - 1796 (2012/01/03)

In this paper, we have shown that the [RuCl2(p-cymene)] 2 complex associated with simple hemisalen ligands is able to racemize (S)-1-phenylethanol. The influence on the racemization process of the ligand's structure as well as the nature of a co-catalyst have been evaluated and optimized. This [RuCl2(p-cymene)]2/Ligand/TEMPO racemization system was then associated with the Candida Antarctica B lipase in order to carry out dynamic kinetic resolution experiments on rac-phenylethanol. This led us to identify the best conditions for effective DKR, which was then applied to various secondary benzylic and aliphatic alcohols. It was thus possible to obtain (R)-1-cyclohexylethyl acetate from rac-1-cyclohexylethanol in quantitative conversion and with high enantioselectivity (98%).

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