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4-Acetylphenyl Ether, also known as PEA or p-acetylphenyl ether, is an organic chemical compound with the empirical formula C10H10O2 and the IUPAC name of 1-(4-ethoxyphenyl)ethan-1-one. It is characterized by a phenyl ring (a circular arrangement of carbon atoms) with an ether and an acetyl group attached. 4-ACETYLPHENYL ETHER is notable for its presence in various types of essential oils.

2615-11-4

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2615-11-4 Usage

Uses

Used in Perfumery Industry:
4-Acetylphenyl Ether is used as a fragrance ingredient for its pleasant aroma. It is predominantly employed in the manufacturing of perfumes, contributing to the unique scents of various products.
Used in Pharmaceutical Industry:
4-Acetylphenyl Ether is used as an intermediate in the synthesis of various pharmaceutical products. Its chemical structure allows it to be a key component in the development of new drugs and medications.
Used in Chemical Industry:
4-Acetylphenyl Ether is used as an intermediate in the synthesis of various chemical products. Its versatile chemical properties make it a valuable compound in the production of different types of chemicals and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 2615-11-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2615-11:
(6*2)+(5*6)+(4*1)+(3*5)+(2*1)+(1*1)=64
64 % 10 = 4
So 2615-11-4 is a valid CAS Registry Number.

2615-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Acetylphenyl ether

1.2 Other means of identification

Product number -
Other names 1-[4-(4-acetylphenoxy)phenyl]ethanone

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:2615-11-4 SDS

2615-11-4Relevant academic research and scientific papers

The role of ancillary ligand on regulating photoluminescence properties of Eu(III) helicates

Gao, Ting,Li, Hongfeng,Ma, Hongjian,Yan, Pengfei,Zhou, Yanyan

, (2021)

Three binuclear Eu3+ helicates, [Eu2(OBTA)3(H2O)3(CH3COCH3)]·1.5CH3COCH3·H2O (1), [Eu2(OBTA)3(Bpy)2]·2CH3/

Investigations into the structure-activity relationship in gemini QACs based on biphenyl and oxydiphenyl linker

Vereshchagin, Anatoly N.,Frolov, Nikita A.,Konyuhova, Valeria Yu,Kapelistaya, Ekaterina A.,Hansford, Karl A.,Egorov, Mikhail P.

, p. 3429 - 3438 (2021/02/03)

Eighteen novel gemini quaternary ammonium compounds were synthesized to examine the effect of linker nature, aliphatic chain length and their relative position on antibacterial and antifungal activity. The synthesized compounds showed strong bacteriostatic activity against a panel of both Gram-positive and Gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and two fungi. Some of these compounds exhibited a wider and more potent antimicrobial spectrum than commonly-used antiseptics, such as benzalkonium chloride (BAC), cetylpyridinium chloride (CPC), chlorhexidine digluconate (CHG) and octenidine dihydrochloride (OCT).

Diaryl Ether Formation Merging Photoredox and Nickel Catalysis

Liu, Le,Nevado, Cristina

supporting information, p. 2188 - 2193 (2021/05/04)

Photoredox and Ni catalysis are combined to produce diaryl ethers under mild conditions. A broad range of aryl halides and phenol derivatives are cross-coupled in the presence of a readily available organic photocatalyst and NiBr2(dtbpy). Symmetrical diaryl ethers have also been directly obtained from aryl bromides in the presence of water. Mechanistic investigations support the involvement of Ni(0) species at the outset of the reaction and a Ni(II)/Ni(III)-photocatalyzed single electron transfer process preceding the productive C(sp2)-OAr reductive elimination.

Nickel-Catalyzed Etherification of Phenols and Aryl Halides through Visible-Light-Induced Energy Transfer

Zhu, Da-Liang,Jiang, Shan,Wu, Qi,Wang, Hao,Li, Hai-Yan,Li, Hong-Xi

supporting information, p. 8327 - 8332 (2021/10/25)

Notwithstanding some progress in nickel-catalyzed etherification of alkanols and arylhalides, the ability of such a Ni-catalyzed transformation employing phenols to diaryl ethers is unsuccessful due to phenolates with much lower reduction potentials, which suppress the oxidation of nickel(II) intermediates into requisite Ni(III) species. We herein report visible-light-initiated, nickel-catalyzed O-arylation of phenols with arylhalides using t-BuNH(i-Pr) as the base and thioxanthen-9-one as the photosensitizer under visible light. This photocoupling exhibits a broad substrate scope.

Selective electrochemical oxidation of aromatic hydrocarbons and preparation of mono/multi-carbonyl compounds

Li, Zhibin,Zhang, Yan,Li, Kuiliang,Zhou, Zhenghong,Zha, Zhenggen,Wang, Zhiyong

, p. 2134 - 2141 (2021/09/29)

A selective electrochemical oxidation was developed under mild condition. Various mono-carbonyl and multi-carbonyl compounds can be prepared from different aromatic hydrocarbons with moderate to excellent yield and selectivity by virtue of this electrochemical oxidation. The produced carbonyl compounds can be further transformed into α-ketoamides, homoallylic alcohols and oximes in a one-pot reaction. In particular, a series of α-ketoamides were prepared in a one-pot continuous electrolysis. Mechanistic studies showed that 2,2,2-trifluoroethan-1-ol (TFE) can interact with catalyst species and generate the corresponding hydrogen-bonding complex to enhance the electrochemical oxidation performance. [Figure not available: see fulltext.]

Selective one-pot access to symmetrical or unsymmetrical diaryl ethers by copper-catalyzed double arylation of a simple oxygen source

Tlili, Anis,Monnier, Florian,Taillefer, Marc

supporting information; experimental part, p. 12299 - 12302 (2011/02/16)

Great CO-mbination: A novel method is reported for the controlled one-pot synthesis of various symmetrical or unsymmetrical diaryl ethers by double arylation of a simple inorganic oxygen source (see scheme). This versatile and highly selective process is based on the use of a cheap and low toxicity copper catalytic system.

Novel bis- and tris-1,2,4-trioxanes: Synthesis and antimalarial activity against multidrug-resistant Plasmodium yoelii in swiss mice

Singh, Chandan,Verma, Ved Prakash,Naikade, Niraj Krishna,Singh, Ajit Shankar,Hassam, Mohammad,Puri, Sunil K.

experimental part, p. 7581 - 7592 (2009/11/30)

A new series of bis-1,2,4-trioxanes 12a-h, 13a-h, and 14a-h and tris-1,2,4-trioxanes 12i-14i were prepared and evaluated against multidrug-resistant Plasmodium yoelii in Swiss mice by oral route. Cyclopentane-based bis-trioxanes 12a, 12b, 12f-h and cycloh

NOVEL SUBSTITUTED BIS-1, 2, 4-TRIOXANES AND A PROCESS FOR PREPARATION THEREOF

-

Page/Page column 10-11, (2008/12/08)

The present invention relates to novel substituted bis-1, 2, 4-trioxanes i.e. compounds containing two 1, 2, 4-trioxane moieties of general formula (6) useful as antimalarial agents. This invention also relates to a process for the preparation of novel su

Synthesis, Structure, Composition, and Properties of Rolivsans

Zaitsev,Khramova,Tsygankova

, p. 634 - 638 (2007/10/03)

Novel thermosetting resins Rolivsans were prepared, and their structure, composition, and properties were studied. The structural parameters of Rolivsans as influenced by the synthesis conditions were determined.

Synthesis of symmetrical diaryl ethers from arylboronic acids mediated by copper(II) acetate

Sagar,Tale,Adude

, p. 7061 - 7063 (2007/10/03)

Copper promoted generation of phenols in situ through arylation of water and their subsequent arylation with arylboronic acids affords a wide range of symmetrical diaryl ethers in good to high yield. The reaction is rapid, mild, convenient and tolerant of a wide range of functionalities on the arylboronic acid.

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