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Benzene, 1-[2-(4-methylphenyl)ethenyl]-4-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156871-45-3

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156871-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156871-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,8,7 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 156871-45:
(8*1)+(7*5)+(6*6)+(5*8)+(4*7)+(3*1)+(2*4)+(1*5)=163
163 % 10 = 3
So 156871-45-3 is a valid CAS Registry Number.

156871-45-3Relevant academic research and scientific papers

Redesign of a Pyrylium Photoredox Catalyst and Its Application to the Generation of Carbonyl Ylides

Alfonzo, Edwin,Alfonso, Felix Steven,Beeler, Aaron B.

supporting information, p. 2989 - 2992 (2017/06/07)

We report the exploration into photoredox generation of carbonyl ylides from benzylic epoxides using newly designed 4-mesityl-2,6-diphenylpyrylium tetrafluoroborate (MDPT) and 4-mesityl-2,6-di-p-tolylpyrylium tetrafluoroborate (MD(p-tolyl)PT) catalysts. These catalysts are excited at visible wavelengths, are highly robust, and exhibit some of the highest oxidation potentials reported. Their utility was demonstrated in the mild and efficient generation of carbonyl ylides from benzylic epoxides that otherwise could not be carried out by current common photoredox catalysts.

Ruthenium-Sulfonamide-Catalyzed Direct Dehydrative Condensation of Benzylic C-H Bonds with Aromatic Aldehydes

Takemoto, Shin,Shibata, Eri,Nakajima, Mitsuaki,Yumoto, Yoshihiro,Shimamoto, Mayuko,Matsuzaka, Hiroyuki

supporting information, p. 14836 - 14839 (2016/11/29)

The first catalytic dehydrative condensation of the benzylic C-H bonds of toluene and p-xylene with aromatic aldehydes is reported herein. This protocol provides highly atom-economical access to stilbene and p-distyrylbenzene derivatives, whereby water is the sole byproduct. The reaction is based on the deprotonation-functionalization of benzylic C-H bonds through η6-complexation of the arenes, which is realized for the first time using a catalytic amount of a transition metal activator. The key to the success of this method is the use of a sulfonamide anion as a catalyst component, which appears to facilitate not only the deprotonation of the benzylic C-H bonds but also the formation of a C-C bonds via an electrophilic tosylimine intermediate.

Heck reactions using segmented flow conditions

Ahmed-Omer, Batoul,Barrow, David A.,Wirth, Thomas

scheme or table, p. 3352 - 3355 (2009/08/17)

Various Heck couplings have been carried out using segmented flow conditions to accelerate the reactions. Aryl iodides and aryl bromides as well as anilines in diazonium-type Heck reactions have been used successfully.

Synthesis and calcium antagonistic activity of diethyl styrylbenzylphosphonates

Younes, S.,Tchani, G.,Baziard-Mouysset, G.,Stigliani, J. L.,Payard, M.,et al.

, p. 87 - 94 (2007/10/02)

Twenty-three new phosphonic ester derivatives of stilbene exhibiting structural analogies with fostedil are described.Examination of calcium antagonism showed that this activity could not be increased by introducing electron-withdrawing, electronreleasing

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