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Benzene, 1,3,5-trimethyl-2-(1-phenyl-1-propenyl)-, (E)-, also known as 1,3,5-trimethyl-2-(1-phenylprop-1-en-1-yl)benzene, is an organic compound characterized by a benzene ring with three methyl groups at the 1, 3, and 5 positions and a 1-phenylprop-1-en-1-yl group at the 2 position. Benzene, 1,3,5-trimethyl-2-(1-phenyl-1-propenyl)-, (E)- is a derivative of benzene, featuring a phenyl group attached to a propenyl chain, which gives it unique chemical properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. The (E)- configuration indicates the geometric arrangement of the double bond in the propenyl group, which can influence the compound's reactivity and physical properties.

4332-15-4

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4332-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4332-15-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,3 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4332-15:
(6*4)+(5*3)+(4*3)+(3*2)+(2*1)+(1*5)=64
64 % 10 = 4
So 4332-15-4 is a valid CAS Registry Number.

4332-15-4Relevant academic research and scientific papers

Microwave-assisted, Pd(0)-catalyzed cross-coupling of diazirines with aryl halides

Zhao, Xia,Wu, Guojiao,Yan, Chong,Lu, Kui,Li, Hui,Zhang, Yan,Wang, Jianbo

supporting information; experimental part, p. 5580 - 5583 (2011/02/23)

Pd(0)-catalyzed cross-coupling reactions of diazirines with aryl halides under microwave heating conditions afford a series of substituted olefins. A reaction mechanism involving the migratory insertion of the Pd carbene intermediate is proposed.

FeCl3-catalyzed alkenylation of simple arenes with aryl-substituted alkynes

Li, Ruoshi,Wang, Sunewang R.,Lu, Wenjun

, p. 2219 - 2222 (2008/02/05)

An addition of electron-rich arenes to aryl-substituted alkynes to form 1,1-diaryl alkenes is carried out in the presence of FeCl3 as catalyst under mild conditions.

Thermodynamically- and kinetically-controlled Friedel-Crafts alkenylation of arenes with alkynes using an acidic fluoroantimonate(v) ionic liquid as catalyst

Choi, Doo Seong,Kim, Jin Hong,Shin, Ueon Sang,Deshmukh, Ravindra R.,Song, Choong Eui

, p. 3482 - 3484 (2008/03/12)

By employing superacidic fluoroantimonate ionic liquid (IL), [bmim][Sb 2F11], as catalyst, not only thermodynamically-controlled but also kinetically-controlled Friedel-Crafts alkenylations of arenes with alkynes have been realized for the first time. The Royal Society of Chemistry.

Gold-catalyzed hydroarylation of alkynes

Reetz, Manfred T.,Sommer, Knut

, p. 3485 - 3496 (2007/10/03)

The hydroarylation of aryl-substituted alkynes by substituted electron-rich arenes is catalyzed by AuCl3 activated by such silver salts as AgSbF6. In the case of terminal alkynes, complete regioselectivity in favor of the 1,1-disubstituted olefin is observed. In the case of electron-poor alkynes such as acetylenecarboxylic acid ester, gold(I) complexes such as [Ph3PAuCl] activated by Ag salts or BF 3·OEt2 are the best catalysts, resulting in opposite regioselectivity and high degrees of (Z)-selectivity. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

Mechanisms of Epoxidation during Ozonation of Carbon-Carbon Double Bonds

Bailey, Philip S.,Hwang, Hank H.,Chiang, Chin-Yun

, p. 231 - 234 (2007/10/02)

Epoxidation of several highly hindered olefins with ozone is stereospecific in all solvents, nucleophilic or nonnucleophilic.This is in agreement with expectations based on the initial formation of a ? rather than an open ? complex.

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