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2,4-dichloro-N-phenylbenzamide, an organic chemical compound with the molecular formula C13H9Cl2NO, is a white crystalline solid that is soluble in organic solvents. It is known for its effectiveness in disrupting the growth and development of plants and insects, making it a valuable component in various applications.

6043-39-6

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6043-39-6 Usage

Uses

Used in Agricultural Industry:
2,4-dichloro-N-phenylbenzamide is used as a herbicide for controlling the growth of unwanted plants, ensuring the healthy development of crops and maximizing agricultural productivity. Its ability to disrupt plant growth makes it an effective tool in this industry.
Used in Pest Control Industry:
In the pest control industry, 2,4-dichloro-N-phenylbenzamide is used as an insecticide to manage and eliminate insect populations that can cause damage to crops and stored products. Its insecticidal properties help protect agricultural produce from pest infestations.
Used in Research and Laboratory Settings:
2,4-dichloro-N-phenylbenzamide is used as a reagent and intermediate in the synthesis of other organic compounds in research and laboratory settings. Its chemical properties make it a valuable component in the development of new chemical entities and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 6043-39-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,4 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6043-39:
(6*6)+(5*0)+(4*4)+(3*3)+(2*3)+(1*9)=76
76 % 10 = 6
So 6043-39-6 is a valid CAS Registry Number.

6043-39-6SDS

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 2,4-dichloro-N-phenylbenzamide

1.2 Other means of identification

Product number -
Other names 2,4-Dichloro-N-phenyl-benzamide

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:6043-39-6 SDS

6043-39-6Relevant academic research and scientific papers

Continuous flow photochemistry as an enabling synthetic technology: Synthesis of substituted-6(5: H)-phenanthridinones for use as poly(ADP-ribose) polymerase inhibitors

Fang,Tranmer

supporting information, p. 720 - 724 (2016/05/19)

Methods utilizing continuous flow photochemistry, an enabling synthetic technology, have been developed for the generation of phenanthridinones via an intramolecular photochemical cyclization of 2-chlorobenzamides for the purposes of generating poly(ADP-ribose) polymerase inhibitors. Herein we report 16 examples of a single-step flow photocyclization which produces substituted phenanthridinones in yields up to 99%, while a two-step method leads directly to phenanthridinones from 2-chlorobenzoyl chlorides and anilines via a novel continuous flow amidation/photocyclization protocol. Overall, the flow photocyclization reactions typically progress in good to excellent yields, and in a superior fashion to analogous batch methods, greatly enabling the drug discovery process.

Metal-free n -arylation of secondary amides at room temperature

Tinnis, Fredrik,Stridfeldt, Elin,Lundberg, Helena,Adolfsson, Hans,Olofsson, Berit

supporting information, p. 2688 - 2691 (2015/06/16)

The arylation of secondary acyclic amides has been achieved with diaryliodonium salts under mild and metal-free conditions. The methodology has a wide scope, allows synthesis of tertiary amides with highly congested aryl moieties, and avoids the regioselectivity problems observed in reactions with (diacetoxyiodo)benzene.

Copper catalysed C-N bond formation via a sequential acylation and deacylation process: A novel strategy for the synthesis of benzanilides

Kumar, Saurabh,Vanjari, Rajeshwer,Guntreddi, Tirumaleswararao,Singh, Krishna Nand

, p. 9920 - 9924 (2015/02/19)

An efficient and mild oxidative amidation of aldehydes by means of acetanilides as amine components has been developed for the first time using copper catalysis. The approach is versatile and proceeds through sequential acylation and deacylation steps to afford benzanilides.

Phosphine-free atmospheric carbonylation of aryl iodides with aniline derivatives in the presence of a reusable silica-supported palladium catalyst

Urbán, Béla,Papp, Máté,Srankó, Dávid,Skoda-F?ldes, Rita

, p. 150 - 157 (2015/02/19)

Various palladium catalysts were obtained by the immobilisation of palladium on silica, modified with imidazolium salts. The efficiency of the catalysts was greatly dependent on the choice of the anion of the imidazolium salt, the palladium precursor and on the conditions of heterogenisation. Palladium acetate immobilised on silica with grafted imidazolium chloride moieties was shown to be a selective and recyclable catalyst for atmospheric aminocarbonylation of aryl iodides with aromatic amines in DMF. It was proved that the greater loss of palladium in DMSO can be explained by the formation of soluble palladium complexes.

Highly efficient dehydrogenative cross-coupling of aldehydes with amines and alcohols

Deshidi, Ramesh,Rizvi, Masood Ahmad,Shah, Bhahwal Ali

, p. 90521 - 90524 (2015/11/11)

A common protocol for the synthesis of amides, esters and α-ketoesters via cross dehydrogenative coupling of aldehydes and amines/alcohols has been developed. The method is applicable to a wide variety of alcohols and amines as well as aliphatic and aromatic aldehydes. Also, the use of acetaldehyde for acetylation and ethyl glyoxalate to access 2-oxo-amino esters is presented for the first time.

SMALL MOLECULE MODIFIERS OF MICRORNA MIR-122

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Page/Page column 38; 40, (2011/08/08)

MicroRNAs are a class of endogenous regulators of gene function. Aberrant regulation of microRNAs has been linked to various human diseases, most importantly cancer. Small molecule intervention of microRNA misregulation has the potential to provide new th

Metal-free synthesis of amides by oxidative amidation of aldehydes with amines in PEG/oxidant system

Liang, Jun,Lv, Jing,Shang, Zhi-Cai

supporting information; experimental part, p. 8532 - 8535 (2011/11/12)

A simple, inexpensive, and efficient one-pot synthesis of amide derivatives were achieved in good to excellent yields via the directly oxidative amidation of aldehydes with amines under PEG/Oxidant system.

Small molecule modifiers of MicroRNA miR-122 function for the treatment of hepatitis C Virus infection and hepatocellular carcinoma

Young, Douglas D.,Connelly, Colleen M.,Grohmann, Christoph,Deiters, Alexander

supporting information; experimental part, p. 7976 - 7981 (2010/08/05)

MicroRNAs are a recently discovered new class of important endogenous regulators of gene function. Aberrant regulation of microRNAs has been linked to various human diseases, most importantly cancer. Small molecule intervention of microRNA misregulation h

Synthesis of amides through the Cannizzaro-type reaction catalyzed by lanthanide chlorides

Zhang, Lijun,Su, Shunpeng,Wu, Hongping,Wang, Shaowu

supporting information; experimental part, p. 10022 - 10024 (2010/02/27)

Amidation of aldehydes with lithium amides through the LnCl3-catalyzed Cannizzaro-type reactions afforded a variety of amides in high yields. The electronic and steric effects on the reaction were investigated. The features of the economical ca

Synthesis of some aryl/heteroaryl tetrazole derivatives and their mass fragmentation study

Dutta, Babul C.,Borthakur, Susanta K.,Goswami, Birendra N.

, p. 565 - 568 (2007/10/03)

Synthesis of some aryl and heteroaryl tetrazole derivatives are described and their electron impact mass fragmentation pattern is discussed.

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