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1-(5-(3-(trifluoromethyl)phenyl)thiophene-2-yl)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

893735-18-7

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893735-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 893735-18-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,3,7,3 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 893735-18:
(8*8)+(7*9)+(6*3)+(5*7)+(4*3)+(3*5)+(2*1)+(1*8)=217
217 % 10 = 7
So 893735-18-7 is a valid CAS Registry Number.

893735-18-7Downstream Products

893735-18-7Relevant academic research and scientific papers

Pd-Catalyzed Functionalization of the Thenoyltrifluoroacetone Coligands by Aromatic Dyes in Bis(cyclometallated) IrIII Complexes: From Phosphorescence to Fluorescence?

Dang, Tung T.,Bonneau, Micka?le,Gareth Williams,Le Bozec, Hubert,Doucet, Henri,Guerchais, Véronique

, p. 2956 - 2964 (2015)

The synthesis, characterization and photophysical properties of a series of neutral Ir(CN-Meppy)2(OO-tta-Ar) (MeppyH = 4-methyl-2-phenylpyridine; tta = thenoyltrifluoroacetonate) complexes containing new functionalized tta-Ar ligands in which the incorporated Ar group is an aromatic dye such as naphthalene, pyrene, naphthalimide or coumarin, are reported. The arylated proligands ttaH-Ar are readily obtained in two steps through Pd-catalyzed C-H bond activation of 2-acetylthiophene. In contrast to the parent Ir(CN)2(OO) complexes, which are phosphorescent in solution at room temperature, all of the arylated complexes display fluorescence, and the phosphorescence emission is quenched. Thus, this work shows that the incorporation of such aromatic dyes in the tta ligand has a dramatic influence on the photophysical properties of the resulting Ir complexes.

Synthesis of functionalized 2-arylthiophenes with triarylbismuths as atom-efficient multicoupling organometallic nucleophiles under palladium catalysis

Rao, Maddali L. N.,Banerjee, Debasis,Dhanorkar, Ritesh J.

supporting information; experimental part, p. 1324 - 1330 (2011/07/07)

Atom-efficient cross-coupling reactions of functionalized 2-bromo- and 2-iodothiophenes have been demonstrated using triarylbismuths as atom-efficient multicoupling organometallic nucleophiles under palladium-catalyzed conditions. These couplings with various functionalized triarylbismuths proceeded smoothly to afford the corresponding functionalized 2-arylthiophenes in high yields. Georg Thieme Verlag Stuttgart · New York.

DERIVATIVES OF SUBSTITUTED 3-PHENYL-1-(PHENYLTHIENYL)PROPAN-1-ONES AND OF 3-PHENYL-1-(PHENYLFURANYL) PROPAN-1-ONES, PREPARATION AND USE

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Page/Page column 14, (2010/03/02)

The present invention relates to compounds derived from substituted 3-phenyl-1-(thien-2-yl)propan-1-ones, pharmaceutical compositions comprising them as well as their therapeutic applications, notably in the field of human and animal health.

Preparation of aryl and heteroaryl indium(III) reagents by the direct insertion of indium in the presence of LiCl

Chen, Yi-Hung,Knochel, Paul

supporting information; experimental part, p. 7648 - 7651 (2009/04/06)

Sensitive functional groups, including ketone, aldehyde, and ester groups, may be present in aryl indium reagents prepared in good to excellent yields by the treatment of aryl and heteroaryl iodides with indium powder in the presence of LiCl (see example)

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