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2-Butenamide, N-(4-methylphenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95152-23-1

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95152-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95152-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,1,5 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 95152-23:
(7*9)+(6*5)+(5*1)+(4*5)+(3*2)+(2*2)+(1*3)=131
131 % 10 = 1
So 95152-23-1 is a valid CAS Registry Number.

95152-23-1Relevant academic research and scientific papers

Regioselective Acetoxylation of Terminal Olefins Using a Palladium(II)–Thiadiazole Catalyst

Li, Xiaohan,Sun, Bin,Zhou, Jiadi,Jin, Can,Yu, Chuangming

supporting information, p. 2635 - 2638 (2019/04/04)

First-time use of a palladium(II)–thiadiazole catalyst in the allylic oxidation of terminal olefins to linear allylic acetates. Employing this strategy, a range of allylic esters (20 examples) were synthesized in 43 % to 80 % yield with excellent regio- and stereoselectivities.

Copper-catalyzed dehydrogenative cross-coupling reactions of N-para-tolylamides through successive C-H activation: Synthesis of 4H-3,1-benzoxazines

Xiong, Tao,Li, Yan,Bi, Xihe,Lv, Yunhe,Zhang, Qian

supporting information; experimental part, p. 7140 - 7143 (2011/09/12)

A novel annulation reaction of readily available tolylamides was catalyzed by Cu(OTf)2 in the presence of Selectfluor and water through successive intermolecular C-H activated dehydrogenative cross-coupling reactions of benzylic methyl C(sp3)-H and aromatic C(sp2)-H bonds, and subsequent intramolecular C-O bond formation (see scheme). Copyright

FOTOQUIMICA DE -TOLUIDIDAS DE ACIDOS αβ-INSATURADOS. INFLUENCIA DE LA ADICION DE CARBONATO POTASICO

Barbera, Carmen,Garcia, Hermenegildo,Miranda, Miguel Angel,Primo, Jaime

, p. 95 - 102 (2007/10/02)

Irradiation of the p-toluidides of crotonic and cinnamic acids (2a,c) gives rise predominantly to the cis isomers 5a,c, together with appreciable amounts of 4,6-dimethyl-3,4-dihydro-2-quinolone (6a) in the case of 2a.The corresponding photo-Fries products have not been detected, even when the irradiation is performed in the presence of K2CO3.By contrast, photolysis of the p-toluidides of methylcrotonic and phenylpropiolic acids (2b,d) gives rise to the o-aminophenones 7b,d (in addition to the quinolone 6b from 2b).For these two amides, as well as for acetanilide and benzanilide, the selectivity towards the acyl migration product markedly increases when the irradiation is performed in the presence of K2CO3.Key words: Enamides' photocyclization, photo-Fries, quinolones.

Synthesis of Benzoquinolizine Derivatives

Merchant, J. R.,Pathare, P. M.

, p. 471 - 472 (2007/10/02)

The reaction of α,β-unsaturated acids with aromatic amines in the presence of PPA affords directly benzo-quinolizines (I).The structures of all the compounds have been established on the basis of elemental analyses and spectral data.

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