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4,4,4-TRIFLUORO-3-HYDROXY-1-PHENYL-BUT-2-EN-1-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41463-86-9

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41463-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41463-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,6 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41463-86:
(7*4)+(6*1)+(5*4)+(4*6)+(3*3)+(2*8)+(1*6)=109
109 % 10 = 9
So 41463-86-9 is a valid CAS Registry Number.

41463-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,4-trifluoro-3-hydroxy-1-phenylbut-2-en-1-one

1.2 Other means of identification

Product number -
Other names 4,4,4-TRIFLUORO-3-HYDROXY-1-PHENYL-BUT-2-EN-1-ONE

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:41463-86-9 SDS

41463-86-9Relevant academic research and scientific papers

Nickel-Catalyzed Aminofluoroalkylation of Alkenes: Access to Difluoroalkylated N-Containing Heterocyclic Compounds

Fu, Xiaoyi,Zhang, Tianyu,Wu, Jingjing,Sun, Yijie,Wu, Fanhong

supporting information, (2021/12/03)

A nickel-catalyzed aminofluoroalkylative cyclization of unactive alkenes with iododifluoromethyl ketones was developed to construct versatile difluoroalkylated Nitrogen-containing heterocycles including aziridines, pyrrolidines and piperidines in moderate to high yields. This method features a broad substrate scope and has been demonstrated on gram scale.

Copper-Catalyzed Three-Component Reactions of 2-Iodo-2,2-difluoroacetophenones, Alkynes, and Trimethylsilyl Cyanide

Wu, Pingjie,Zheng, Cheng,Wang, Xia,Wu, Jingjing,Wu, Fanhong

supporting information, p. 1420 - 1423 (2021/02/01)

A Cu(I)-catalyzed three-component reaction of 2-iodo-2,2-difluoroacetophenones, alkynes, and TMSCN is described. The reaction provided a facile method for the synthesis of difluoroacyl-substituted nitriles, which might be served as potentially useful fluo

Preparation method of gamma-bromine-beta, gamma-alkenyl fluoroketone derivatives

-

Paragraph 0026-0028, (2021/01/30)

The invention relates to a preparation method of gamma-bromine-beta, gamma-alkenyl fluoroketone derivatives, which comprises the following steps: dissolving a compound represented by formula (IV) andcorresponding alkyne in acetone, adding bis (triphenylph

A accompanies two fluorine substituted tetrahydronaphthalene ketone compound and its preparation method

-

Paragraph 0034; 0036; 0042; 0044; 0049; 0051, (2019/07/04)

The invention provides a accompanies two fluorine substituted tetrahydronaphthalene ketone compound and its preparation method. The accompanies two fluorine substituted tetrahydronaphthalene ketone compound, characterized in that its structure such as for

Nickel-Catalyzed Coupling Reaction of α-Bromo-α-fluoroketones with Arylboronic Acids toward the Synthesis of α-Fluoroketones

Liang, Junqing,Han, Jie,Wu, Jingjing,Wu, Pingjie,Hu, Jian,Hu, Feng,Wu, Fanhong

supporting information, p. 6844 - 6849 (2019/09/07)

A nickel-catalyzed coupling reaction of α-bromo-α-fluoroketones with arylboronic acids was reported, which provides an efficient pathway to access 2-fluoro-1,2-diarylethanones in high yields. We also disclosed the synthesis of the monofluorination agents

Beta-iododifluoroacetone derivative and preparation method thereof

-

Paragraph 0035; 0036; 0038; 0039, (2020/01/12)

The invention relates to a beta-iododifluoroacetone derivative and a preparation method thereof. The preparation method comprises the following steps: dissolving an iododifluoroketone compound raw material and an olefin raw material in a solvent, then add

Palladium-Catalyzed Benzodifluoroalkylation of Alkynes: A Route to Fluorine-Containing 1,1-Diarylethylenes

Liang, Junqing,Huang, Guozhi,Peng, Peng,Zhang, Tianyu,Wu, Jingjing,Wu, Fanhong

supporting information, p. 2221 - 2227 (2018/04/17)

A palladium(0)-catalyzed three-component reaction of 2-iodo-2,2-difluoroacetophenones, alkynes and arylboronic acids is introduced for the synthesis of 1-benzoyldifluoromethyl-2,2-diphenylethylenes in good yields and with excellent stereoselectivity. The

Detrifluoroacetylation Reaction of Trifluoromethyl-β-diketones: Facile Method for the Synthesis of Succinimide Derivatives and 1,4-Diketones

Wang, Li-Hua,Zhao, Jing

supporting information, p. 4345 - 4348 (2018/08/31)

Currently, a great deal of research efforts are focused on C–C bond activation for development of novel synthetic methodology. In this paper, a detrifluoroacetylation of trifluoromethyl-β-diketones is described, which allows for the synthesis of succinimides and 1,4-diketones through cascade Michael addition/retro-Claisen reaction and nucleophilic substitution/retro-Claisen reaction. The readily available trifluoromethyl-β-diketones, wide substrate scope, and mild conditions make this method very practical.

Synthesis of α,α-difluorobenzoyl oxygen heterocycles via the radical reaction of 2-iodo-2,2-difluoroacetophenones with unsaturated acids or unsaturated alcohols

Chen, Heng,Wang, Jiexiong,Wu, Jingjing,Kuang, Yujia,Wu, Fanhong

, p. 41 - 46 (2017/06/14)

A convenient and facile method for the direct synthesis of α,α-difluorobenzoyl lactones or cyclic ethers via the radical cyclization reaction of 2-iodo-2,2-difluoroacetophenone with unsaturated acids or alcohols was reported.

Palladium-catalyzed direct mono-α-arylation of α-fluoroketones with aryl halides or phenyl triflate

Zhou, Jun,Fang, Xiang,Shao, Tongle,Yang, Xueyan,Wu, Fanhong

supporting information, p. 54 - 62 (2016/10/05)

A palladium catalyzed Negishi-type α-arylation of α-fluoroketones with electron-rich and electron-deficient aryl halides or phenyl triflate has been developed. This direct mono-α-arylation method generate a variety of ternary α-aryl-α-monofluoroketones easily in good to excellent yields using XPhos as ligand and Cs2CO3as mild base.

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