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1-methoxy-4-[(4-nitrophenoxy)methyl]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31574-13-7

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31574-13-7 Usage

Physical appearance

White crystalline solid 1-methoxy-4-[(4-nitrophenoxy)methyl]benzene appears as a white, crystalline solid substance.

Usage in pharmaceuticals and agrochemicals

Production 1-methoxy-4-[(4-nitrophenoxy)methyl]benzene is used in the production of various pharmaceuticals and agrochemicals due to its chemical properties.

Chemical structure

Benzene ring with methoxy and nitro groups The compound has a benzene ring core with a methoxy group (-OCH3) and a nitro group (-NO2) attached to it.

Additional functional group

Phenoxy methyl group Along with the methoxy and nitro groups, 1-methoxy-4-[(4-nitrophenoxy)methyl]benzene also has a phenoxy methyl group (-OCH2C6H4) in its structure.

Organic synthesis

Building block 1-methoxy-4-[(4-nitrophenoxy)methyl]benzene is commonly used as a building block in organic synthesis, making it a versatile chemical in the creation of other compounds.

Medical properties

Anti-inflammatory and analgesic 1-methoxy-4-[(4-nitrophenoxy)methyl]benzene is known to exhibit anti-inflammatory and analgesic (pain-relieving) properties.

Intermediate in chemical synthesis

Dyes and pigments The compound is also used as an intermediate in the synthesis of other chemicals, such as dyes and pigments.

Precaution

Potential hazards to human health and environment It is important to handle 1-methoxy-4-[(4-nitrophenoxy)methyl]benzene with caution, as it may pose hazards to both human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 31574-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,5,7 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 31574-13:
(7*3)+(6*1)+(5*5)+(4*7)+(3*4)+(2*1)+(1*3)=97
97 % 10 = 7
So 31574-13-7 is a valid CAS Registry Number.

31574-13-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-4-[(4-nitrophenoxy)methyl]benzene

1.2 Other means of identification

Product number -
Other names 1-(4-nitrophenoxymethyl)-4-methoxybenzene

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:31574-13-7 SDS

31574-13-7Relevant academic research and scientific papers

Structure based design, synthesis, and biological evaluation of imidazole derivatives targeting dihydropteroate synthase enzyme

Daraji, Drashti G.,Rajani, Dhanji P.,Rajani, Smita D.,Pithawala, Edwin A.,Jayanthi, Sivaraman,Patel, Hitesh D.

supporting information, (2021/02/16)

In this study, we have designed and synthesized 2-((5-acetyl-1-(phenyl)-4-methyl-1H-imidazol-2-yl)thio)-N-(4-((benzyl)oxy)phenyl) acetamide derivatives. Antimicrobial activities of all the imidazole derivatives have been examined against Gram-positive and Gram-negative bacteria and results showed that the conjugates have appreciable antibacterial activity. Besides, several analogous were evaluated for their in vitro antiresistant bacterial strains such as Extended-spectrum beta-lactamases (ESBL), Vancomycin-resistant Enterococcus (VRE), and Methicillin-resistant Staphylococcus aureus (MRSA). The SAR revealed that the 12l compound resulted in potency against all bacterial strains as well as ESBL, VRE, and MRSA strains. Lipinski's rule of five, and ADME studies were preformed for all the synthesized compounds with Staphylococcus aureus dihydropteroate synthase (saDHPS) protein (PDB ID: 6CLV) and were found standard drug-likeness properties of conjugates. Moreover, the binding mode of the ligands with the protein study has been examined by molecular docking and results are quite promising. Besides, all the analogous were tested for their in vitro antituberculosis, antimalarial, and antioxidant activity.

Method for synthesizing aryl benzyl ether compound

-

Paragraph 0038; 0041, (2021/04/14)

The invention discloses a method for synthesizing aryl benzyl ether compounds, which comprises the following steps: by using an iron (III) complex containing 1, 3-di-tert-butyl imidazole cations and having a molecular formula of [(tBuNCH = CHNtBu) CH] [FeBr4] as a catalyst and di-tert-butyl peroxide as an oxidant, carrying out oxidative coupling reaction on phenolic compounds and toluene compounds to synthesize the corresponding aryl benzyl ether compounds. The method is the first example for preparing the aryl benzyl ether compound through the oxidative coupling reaction of the phenolic compound and the toluene compound, which is realized by an iron-based catalyst, and has the advantages of atom economy, environmental friendliness and good substrate applicability.

Application of iron (III) complex containing 1,3-di-tert-butyl imidazole cations in synthesis of aryl benzyl ether compounds

-

Paragraph 0037-0038, (2021/04/26)

The invention discloses an application of an iron (III) complex containing 1,3-di-tert-butyl imidazole cations in synthesis of aryl benzyl ether compounds, and particularly relates to a method for synthesizing corresponding aryl benzyl ether compounds by taking di-tert-butyl peroxide as an oxidizing agent and carrying out oxidative coupling reaction on phenolic compounds and toluene compounds. According to the method, the iron (III) complex is used as the catalyst for the first time, and oxidative coupling of the phenolic compound and the toluene compound is realized. The method is the first oxidative coupling reaction of phenolic compounds and benzyl C(sp3)-H bonds, and a new method is provided for synthesizing aryl benzyl ether compounds. Compared with an existing synthesis method, the method provided by the invention avoids using toxic and polluting halogenated hydrocarbon and strong base, has better atom economy, and conforms to the development concept of green synthetic chemistry.

Applicability of aluminum amalgam to the reduction of arylnitro groups

Luzzio, Frederick A.,Monsen, Paige J.

supporting information, (2020/11/02)

An array of arylnitro compounds with various functionality were treated with freshly-prepared aluminum amalgam in THF/water solution and resulted in the corresponding arylamines. The Al(Hg)-mediated reductions are relatively rapid with consumption of the amalgam and disappearance of starting material occurring over 20–30 min. The workup of the reductions involves only removal of the insoluble by-products by filtration followed by concentration. Only in some cases is chromatography required to secure the pure product. The desired arylamines are furnished in quantities of 25–100 mg, which in some cases, could be taken on to the next reaction without further purification. Reductions of 4-nitrobenzyl derivatives of carbohydrates or nucleosides were selective in affording the corresponding 4-aminobenzyl products. To show applicability in click chemistry, selected aminobenzyl products are directly azidated to yield products that were then used in click reactions to afford the corresponding 1,2,3-triazoles.

Aryl Ether Syntheses via Aromatic Substitution Proceeding under Mild Conditions

Ando, Shin,Tsuzaki, Marina,Ishizuka, Tadao

, p. 11181 - 11189 (2020/10/12)

In this study, mild conditions for aromatic substitutions during the syntheses of aryl ethers were developed. In the reaction conditions, the choices of solvent, base, and the sequence for the addition of the reagents proved important. A wide variety of alcohols were used directly as nucleophiles and smoothly reacted with aryl chlorides that possessed either a nitro or a cyano group at either the ortho- or para-position. Controlled experiments we performed suggested that the reaction underwent a charge-transfer process mediated by a combination of DMF and tert-BuOK.

Facile and selective deprotection of PMB ethers and esters using oxalyl chloride

Ilangovan, Andivelu,Anandhan, Karnambaram,Kaushik, Mahabir Prasad

supporting information, p. 1081 - 1084 (2015/02/19)

Oxalyl chloride, (0.5 equiv) was found to cleave the PMB group from alkyl, aryl PMB ethers, and esters to give corresponding alcohol and acid in good yields. This method offers simple and efficient protocol for the selective deprotection of PMB ether and ester in DCE at ambient temperature.

Silver(I)-Catalyzed deprotection of p -methoxybenzyl ethers: A mild and chemoselective method

Kern, Nicolas,Dombray, Thomas,Blanc, Aurelien,Weibel, Jean-Marc,Pale, Patrick

, p. 9227 - 9235,9 (2012/12/12)

The p-methoxybenzyl protecting group (PMB) on various alcohols and an acid was efficiently and selectively cleaved by the action of a catalytic amount of silver(I) hexafluoroantimonate combined with 0.5 equiv of 1,3,5- trimethoxybenzene in dichloromethane at 40 °C.

Studies on novel 2-imidazolidinones and tetrahydropyrimidin-2(1H)-ones as potential TACE inhibitors: Design, synthesis, molecular modeling, and preliminary biological evaluation

DasGupta, Shirshendu,Murumkar, Prashant R.,Giridhar, Rajani,Yadav, Mange Ram

experimental part, p. 3604 - 3617 (2009/09/30)

Compounds belonging to the class of 2-imidazolidinones and tetrahydropyrimidin-2(1H)-ones were synthesized and evaluated for their TACE inhibitory activity. Most of the compounds showed very good TACE inhibitory activity. Docking study clearly indicates importance of the P1′ group of the inhibitor for the TACE inhibitory activity. This work proves that these two classes of molecules could be used as potential leads for the development of TACE inhibitors.

Lewis Acid-Catalyzed Deprotection of p-Methoxybenzyl Ether

Bouzide, Abderrahim,Sauvé, Gilles

, p. 1153 - 1154 (2007/10/03)

The p-methoxybenzyl protecting group was readily removed from alcohols and phenols using catalytic amounts of AlCl3 or SnCl2 · 2H2O in the presence of EtSH at room temperature. Under these mild conditions other protecting groups such as methyl and benzyl ethers, p-nitrobenzoyl esters, TBDPS ethers and isopropylidene acetal were unchanged.

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