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1-(4-Bromophenoxy)-2-propanone, with the molecular formula C9H9BrO2, is a chemical compound that features a propanone (acetone) group linked to a phenyl ring with a bromine atom at the para position. This versatile intermediate is widely utilized in organic synthesis and serves as a building block for the development of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique properties and reactivity contribute to its significance in medicinal chemistry and chemical research.

18621-22-2

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18621-22-2 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-Bromophenoxy)-2-propanone is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of a broad range of medicinally relevant molecules, making it an essential component in drug discovery and development.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(4-Bromophenoxy)-2-propanone is employed as a building block for the production of various agrochemicals. Its reactivity and structural properties enable the development of compounds with specific pesticidal, herbicidal, or fungicidal activities, contributing to the advancement of crop protection strategies.
Used in Specialty Chemicals:
1-(4-Bromophenoxy)-2-propanone is also utilized in the synthesis of specialty chemicals, which are tailored for specific applications in various industries. Its unique properties and reactivity make it a valuable component in the development of high-performance materials, additives, and other advanced chemical products.
Used in Medicinal Chemistry Research:
As a compound with potential applications in medicinal chemistry, 1-(4-Bromophenoxy)-2-propanone is used in research to explore its properties and reactivity. This helps scientists understand its potential as a precursor to new therapeutic agents and contributes to the advancement of knowledge in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 18621-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,2 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18621-22:
(7*1)+(6*8)+(5*6)+(4*2)+(3*1)+(2*2)+(1*2)=102
102 % 10 = 2
So 18621-22-2 is a valid CAS Registry Number.

18621-22-2SDS

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 1-(4-bromophenoxy)propan-2-one

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:18621-22-2 SDS

18621-22-2Relevant academic research and scientific papers

Iridium-catalyzed enantioselective intramolecular hydroarylation of allylic aryl ethers devoid of a directing group on the aryl group

Kusaka, Satoshi,Ohmura, Toshimichi,Suginome, Michinori

supporting information, p. 13542 - 13545 (2021/12/23)

Although intramolecular hydroarylation is an attractive transformation of allylic aryl ethers, it has suffered from narrow substrate scope. We herein describe Ir/(S)-DTBM-SEGPHOS-catalyzed intramolecular hydroarylation of allylic aryl ethers. The reaction

Pharmacological profiling of JME-173, a novel mexiletine derivative combining dual anti-inflammatory/anti-spasmodic functions and limited action in Na+ channels

Amendoeira, Fábio Coelho,Araújo, Jo?o Felipe Garcia,Carvalho, Katharinne Ingrid Moraes de,Costa, Jorge Carlos Santos da,Coutinho, Diego de Sá,Faria, Robson Xavier,Ferrero, Maximiliano R.,Fonseca, Laís Bastos da,Martins, Marco Aurélio,Pereira, Heliana Martins,Pinto, Douglas Pereira,Santos-Filho, Osvaldo Andrade,Silva, Aline C. A.,Silva, Diego Medeiros da,Silva, Emerson Teixeira da,Silva, Letícia Vallim da,Silveira, Gabriel Parreiras Estolano,Souza, Marcus Vinicius Nora de

supporting information, (2020/08/21)

Existing evidence suggests that the local anaesthetic mexiletine can be beneficial for patients with asthma. However, caution is required since anaesthesia of the airways inhibits protective bronchodilator neuronal reflexes, limiting applications in condi

Selective Cross-Dehydrogenative C(sp3)-H Arylation with Arenes

Hao, Hong-Yan,Mao, Yang-Jie,Xu, Zhen-Yuan,Lou, Shao-Jie,Xu, Dan-Qian

supporting information, p. 2396 - 2402 (2020/03/13)

Selective C(sp3)-C(sp2) bond construction is of central interest in chemical synthesis. Despite the success of classic cross-coupling reactions, the cross-dehydrogenative coupling between inert C(sp3)-H and C(sp2)-H bonds represents an attractive alternative toward new C(sp3)-C(sp2) bonds. Herein, we establish a selective inter-and intramolecular C(sp3)-H arylation of alcohols with nondirected arenes that thereby provides a general pathway to access a wide range of β-arylated alcohols, including tetrahydronaphthalen-2-ols and benzopyran-3-ols, with high to excellent chemo-and regioselectivity.

TBAI/TBHP mediated oxidative cross coupling of ketones with phenols and carboxylic acids: Direct access to benzofurans

Santhosh Kumar,Ravikumar,Chinna Ashalu,Rajender Reddy

supporting information, p. 33 - 37 (2017/12/11)

TBAI/TBHP mediated oxidative cross coupling of phenols and carboxylic acids with ketones has been reported under metal-free, base free, solvent free conditions enabling environmentally benign synthesis of aryloxyketones, acyloxy ketones and benzofurans. Phenoxyketones and acyloxylcarbonyl compounds were synthesized in good to high yields, where as benzofurans were synthesized in moderate yields. This method is operationally simple, works under mild conditions, using commercially available as well as inexpensive TBAI and an oxidant TBHP.

Photocatalytic Oxidative Bromination of Electron-Rich Arenes and Heteroarenes by Anthraquinone

Petzold, Daniel,K?nig, Burkhard

supporting information, p. 626 - 630 (2017/11/22)

The estimated excited oxidation potential of sodium anthraquinone-2-sulfonate (SAS) increases from 1.8 V to about 2.3 V vs SCE by protonation with Br?nsted acids. This increased photooxidation power of protonated anthraquinone was used for the regio-selective oxidative bromination of electron rich (hetero)arenes and drugs in good yield. The mild reaction conditions are compatible with many functional groups, such as double and triple bonds, ketones, amides and amines, hydroxyl groups, carboxylic acids and carbamates. Mechanistic investigations indicate the photooxidation of the arene followed by nucleophilic bromide addition as the likely pathway. (Figure presented.).

A (different) bright ammonia amide carbamate derivative and application thereof (by machine translation)

-

Paragraph 0036; 0037; 0038; 0049; 0050, (2017/07/14)

The invention belongs to the field of plant, relates to a general formula (I) is shown in a (different) bright ammonia amide carbamate derivatives and their pharmaceutically acceptable salt, wherein substituent R has the definition given in the specification, the invention also relates to the general formula (I) preparation of compounds of the, specifically for the preparation of the intermediate of its development and application of plant disease control. (by machine translation)

Design, synthesis and effect of the introduction of a propargyloxy group on the fungicidal activities of 1-substituted phenoxypropan-2-amino valinamide carbamate derivatives

Li, Jian-Qiang,Wang, Zhi-Peng,Gao, Yang,Zhao, Wei-Guang

, p. 82131 - 82137 (2016/09/09)

The cell walls of oomycetes are composed of cellulose, making cellulose synthase enzymes good targets for carboxylic acid amide fungicides. Valinamide carbamates are amino acid fungicides that represent excellent alternatives to conventional synthetic pesticides in terms of their ability to reduce the negative impacts of these compounds on human health and the environment. In a continuation of our research towards the development of new cellulose synthase inhibitors, we have developed a series of "stretched" analogues of iprovalicarb by the introduction of an additional OCH2 linker. The bioassay results indicated that compounds containing a small group at the para-position of phenyl gave excellent fungicidal activities with EC50 values ranging from 0.59 to 2.06 μmol L-1. Most notably, the introduction of a propargyloxy group led to a pronounced increase in the fungicidal activity. Furthermore, compound 7o bearing a propargyloxy group was identified as the most promising candidate because of its excellent fungicidal potency against oomycete diseases and good fungicidal activity against non-oomycete diseases.

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