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(E)-3-(4-bromophenyl)-4,4,4-trifluoro-1-phenyl-2-buten-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1245905-80-9

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1245905-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1245905-80-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,9,0 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1245905-80:
(9*1)+(8*2)+(7*4)+(6*5)+(5*9)+(4*0)+(3*5)+(2*8)+(1*0)=159
159 % 10 = 9
So 1245905-80-9 is a valid CAS Registry Number.

1245905-80-9Relevant academic research and scientific papers

Catalytic Enantioselective Conjugate Alkynylation of β-Aryl-β-trifluoromethyl Enones Constructing Propargylic All-Carbon Quaternary Stereogenic Centers

Sanz-Marco, Amparo,Blay, Gonzalo,Vila, Carlos,Pedro, José R.

supporting information, p. 3538 - 3541 (2016/08/16)

The enantioselective conjugate alkynylation of β-aryl-β-trifluoromethyl enones has been carried out using terminal alkynes and diethylzinc in the presence of 3,3′-bis(perfluorophenyl)BINOL as the chiral ligand to give the corresponding ketones bearing a t

Synthesis of β-CF3 ketones from trifluoromethylated allylic alcohols by ruthenium catalyzed isomerization

Bizet, Vincent,Pannecoucke, Xavier,Renaud, Jean-Luc,Cahard, Dominique

supporting information, p. 56 - 61 (2013/11/06)

This work describes the optimization process for the synthesis of β-trifluoromethylated ketones from trifluoromethylated allylic alcohols. This transformation proceeds through a ruthenium catalyzed isomerization under mild conditions with high atom econom

Ruthenium-catalyzed redox isomerization of trifluoromethylated allylic alcohols: Mechanistic evidence for an enantiospecific pathway

Bizet, Vincent,Pannecoucke, Xavier,Renaud, Jean-Luc,Cahard, Dominique

supporting information; experimental part, p. 6467 - 6470 (2012/07/27)

Transfer news: A synthetic approach to chiral β-CF3- substituted saturated carbonyl compounds has been developed in which ruthenium complexes efficiently catalyze the redox isomerization of CF3-bearing allylic alcohols by an intramol

Enantioselective synthesis of trifluoromethyl-substituted 2-isoxazolines: Asymmetric hydroxylamine/enone cascade reaction

Matoba, Kazutaka,Kawai, Hiroyuki,Furukawa, Tatsuya,Kusuda, Akihiro,Tokunaga, Etsuko,Nakamura, Shuichi,Shiro, Motoo,Shibata, Norio

supporting information; experimental part, p. 5762 - 5766 (2010/11/03)

(Figure Presented) Cuts both ways: The title reaction consists of an addition/cyclization/dehydration sequence and affords the biologically important chiral 3,5-diaryl-5-(trifluoromethyl)-2-isoxazolines 1 in excellent yields with high ee values. The flexi

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