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[2-(4-bromophenyl)-2-oxoethyl](triphenyl)phosphonium is a phosphonium salt characterized by a phosphorus atom bonded to three phenyl groups and a bromophenyl and an oxoethyl moiety. [2-(4-bromophenyl)-2-oxoethyl](triphenyl)phosphonium is recognized for its strong nucleophilic properties and unique structural features, making it a versatile reactant in organic synthesis.

2928-58-7

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2928-58-7 Usage

Uses

Used in Organic Synthesis:
[2-(4-bromophenyl)-2-oxoethyl](triphenyl)phosphonium is used as a reactant in organic synthesis for its strong nucleophilic properties, which facilitate various chemical reactions and contribute to the formation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [2-(4-bromophenyl)-2-oxoethyl](triphenyl)phosphonium is used as a building block for the synthesis of complex organic molecules with potential therapeutic applications. Its unique reactivity and structural properties make it a valuable component in the development of new pharmaceutical compounds.
Used in Material Industry:
[2-(4-bromophenyl)-2-oxoethyl](triphenyl)phosphonium is also utilized in the material industry, where its structural properties and reactivity are harnessed to create novel materials with specific characteristics for various applications.
Used in Catalyst Development:
[2-(4-bromophenyl)-2-oxoethyl](triphenyl)phosphonium has been investigated for its potential application in the development of new organic catalysts, which are essential for enhancing the efficiency and selectivity of chemical reactions in various industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 2928-58-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,2 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2928-58:
(6*2)+(5*9)+(4*2)+(3*8)+(2*5)+(1*8)=107
107 % 10 = 7
So 2928-58-7 is a valid CAS Registry Number.

2928-58-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(4-bromophenyl)-2-oxoethyl]-triphenylphosphanium

1.2 Other means of identification

Product number -
Other names 1-(4-Bromophenyl)-2-(triphenylphosphoranyl)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:2928-58-7 SDS

2928-58-7Relevant academic research and scientific papers

Substituent effects in the formation of a few acenaphthenone-2-ylidene ketones and their molecular docking studies and in silico ADME profile

A, Jesna,Jacob, Jomon P.,Kuriakose, Daly,Thumpakara, Roshini K.

, (2020/09/15)

We observed intriguing substituent effects in the reaction between 4-substituted acetophenones and acenaphthenequinone in the presence of KOH in methanol. In all cases, expected Claisen-Schimdt condensation was the first step. However, depending on the nature of 4-substituent on acetophenone, the initially formed condensation product remain unchanged or underwent Domino sequence of reactions to give three different 2:2 adducts arising through three distinct pathways. The interactions of acenaphthenone-2-ylidene ketones with the target proteins were performed by molecular docking studies. The prediction of in silico ADME belongings of the synthesized compounds revealed substantial drug-likeness characters based on Lipinski's rules.

Rh(iii)-catalyzed diastereoselective cascade annulation of enone-tethered cyclohexadienonesviaC(sp2)-H bond activation

Chegondi, Rambabu,Jadhav, Sandip B.,Maurya, Sundaram,Navaneetha, N.

supporting information, p. 13598 - 13601 (2021/12/23)

Herein, we report highly diastereoselective arylative cyclization of enone-tethered cyclohexadienonesviaRh(iii)-catalyzed C-H activation ofN-methoxybenzamides. This reaction proceeds through the formation of a five-membered rhodacycle followed by bis-Michael cascade annulation to access functionalized bicyclic scaffolds with four contiguous stereocenters with a broad substrate scope. These products have excellent functional handles, allowing further synthetic transformation to increase the structural complexity. Furthermore, mechanistic studies of arylative cyclization and a gram-scale experiment are also presented.

One-pot synthesis of new hydantoin (thiohydantoin) derivatives and evaluation of their antibacterial and antioxidant activities

Ghasempour, Leila,Asghari, Sakineh,Tajbakhsh, Mahmood,Mohseni, Mojtaba

, p. 4136 - 4148 (2020/09/09)

One-pot four-component reactions of phenacyl bromides, parabanic or thioparabanic acids, thiophenols, and triphenylphosphine in the presence of triethylamine afforded new derivatives of hydantoin or thiohydantoin in good to high yields (65%-90%). Their an

One-Pot Synthesis of 2,5-Disubstituted Furans through In Situ Formation of Allenes and Enolization Cascade

Bernhard, Yann,Gilbert, Joachim,Bousquet, Till,Favrelle-Huret, Audrey,Zinck, Philippe,Pellegrini, Sylvain,Pelinski, Lydie

supporting information, p. 7870 - 7873 (2019/12/24)

A one-pot synthesis of 2,5-disubstituted furans from γ-ketoacids is reported. In situ formation of allenoates by action of chloroformate on carboxylic acid following by enolization of ketone affords furan derivatives by cyclization. The reaction was extended to a wide scope of ketoacids and phosphonium salts. This methodology was applied on levulinic acid and derivatives, one of the biosourced platform chemicals.

PYRROLIDINE DERIVATIVES AS PPAR AGONISTS

-

Paragraph 0738-0741, (2019/08/02)

The present invention discloses a class of pyrrolidine derivatives as PPAR agonist, and their use for the treatment of some diseases of PPAR receptor-associated pathways (such as nonalcoholic steatohepatitis and concurrent fibrosis, insulin resistance, primary biliary cholgangitis, dyslipidenmia, hyperlipidemia, hypercholesterolemia, atherosclerosis, hypertriglyceridemia, cardiovascular disease, obesity or the like). In particular, the present invention discloses a compound represented by Formula (I) or a pharmaceutically acceptable salt thereof.

Fe-Catalyzed Cycloisomerization of Aryl Allenyl Ketones: Access to 3-Arylidene-indan-1-ones

Teske, Johannes,Plietker, Bernd

supporting information, p. 2257 - 2260 (2018/04/27)

A cycloisomerization of aryl allenyl ketones to 3-arylidene-indan-1-ones using a cationic Fe-complex as a catalyst is reported. The catalyst opens a synthetically interesting reaction pathway to this surprisingly underrepresented class of indanones that are not accessible using alternative catalytic systems.

Potassium 2-oxo-3-enoates as Effective and Versatile Surrogates for α, β-Unsaturated Aldehydes in NHC-Catalyzed Asymmetric Reactions

Gao, Yaru,Ma, Yafei,Xu, Chen,Li, Lin,Yang, Tianjian,Sima, Guoqing,Fu, Zhenqian,Huang, Wei

supporting information, p. 479 - 484 (2017/12/26)

Potassium 2-oxo-3-enoates, which are readily prepared at scale and easily stored, have been found to be effective and versatile surrogates for α,β-unsaturated aldehydes in NHC-catalyzed asymmetric reactions. Promoted by chiral N-heterocyclic carbenes combined with LiCl, these easy-to-handle solid salts could release of CO2 and then undergo asymmetric reactions via homoenolate and α, β-unsaturated acyl azolium intermediate. The reactions have broad substrate scopes with high enantioselectivities. (Figure presented.).

Synthesis of trifluoromethyl-/cyclopropyl-substituted 2-isoxazolines by DBU-promoted domino reaction

Liu, Xiao-Dong,Ma, Hai-Yan,Xing, Chun-Hui,Lu, Long

supporting information, p. 1780 - 1783 (2017/07/27)

NTrifluoromethyl and cyclopropyl substituted 2-isoxazolines were synthesized via a DBU-promoted domino reaction of β-trifluoromethyl-/β-cyclopropyl-substituted enones with hydroxylamine. The domino reaction consists of a Michael addition and the followed cyclization. A wide range of 3-substituted 5-cyclopropyl-5- trifluoromethyl-2-isoxazolines were obtained in good to excellent yields under mild reaction conditions. The method could also apply to other trifluoromethyl-substituted enones.

A convenient synthesis of 4-alkyl-3-benzoylpyrroles from α,β-unsaturated ketones and tosylmethyl isocyanide

Kumar, Kapil,More, Shital S.,Goyal, Sandeep,Gangar, Mukesh,Khatik, Gopal L.,Rawal, Ravindra K.,Nair, Vipin A.

supporting information, p. 2315 - 2319 (2016/05/10)

A convenient synthesis of 4-alkyl-3-benzoyl pyrrole was achieved from α,β-unsaturated ketones and tosylmethyl isocyanide in the presence of mild base LiOH·H2O. This method is very economical and was successfully utilized for the synthesis of various 4-alkyl-3-benzoylpyrrole derivatives with good to excellent yields.

Enantioselective Organocatalytic Cascade Approach to Different Classes of Benzofused Acetals

Paz, Bruno Matos,Klier, Lydia,N?sborg, Line,Lauridsen, Vibeke Henriette,Jensen, Frank,J?rgensen, Karl Anker

supporting information, p. 16810 - 16818 (2016/11/16)

A novel enantioselective organocatalytic strategy is presented for the synthesis of tetrahydrofurobenzofuran and methanobenzodioxepine natural product core structures. The strategy is based on a pair of divergent reaction pathways in which hydroxyarenes react with γ-keto-α,β-unsaturated aldehydes, catalyzed by a chiral secondary amine. One reaction pathway, which leads to chiral 5,5-fused acetals with two stereocenters—the tetrahydrofurobenzofuran scaffolds—proceeds in moderate yields and up to 96 % ee. The other reaction pathway provides 5,6-bridged methanobenzodioxepine scaffolds with three stereocenters in moderate to good yields and up to 95 % ee. The reaction is remarkable as it can proceed with catalyst loadings as low as 0.25 mol %, providing one of the highest known turnover numbers in iminium ion catalysis. Furthermore, the hemiacetal tetrahydrofurobenzofuran can undergo functionalizations including reduction, oxidation, and allylation. Finally, the effects involved in the substrate control for the divergent pathways, based on both experimental and computational studies, have been investigated. A model involving steric, electronic and stereoelectronic interactions is discussed to rationalize the observed selectivities.

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