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Benzene, 1,1',1''-(1,2-propadien-1-yl-3-ylidene)tris-, also known as 1,3,5-tri(1,2-propadienyl)benzene, is an organic compound with the chemical formula C12H12. It is a derivative of benzene, where three allyl groups (1,2-propadien-1-yl) are attached to the benzene ring at the 1, 3, and 5 positions. Benzene, 1,1',1''-(1,2-propadien-1-yl-3-ylidene)tris- is characterized by its symmetrical structure and the presence of three conjugated double bonds in the allyl groups, which contribute to its unique electronic properties. It is an important intermediate in the synthesis of various organic compounds and polymers, such as polystyrene and styrene-based copolymers. Due to its reactive nature, it is often used in the production of plastics, resins, and rubber.

966-87-0

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966-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 966-87-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 966-87:
(5*9)+(4*6)+(3*6)+(2*8)+(1*7)=110
110 % 10 = 0
So 966-87-0 is a valid CAS Registry Number.

966-87-0Relevant academic research and scientific papers

Catalytic Electrophilic Thiocarbocyclization of Allenes

Jiang, Quanbin,Li, Huimin,Zhao, Xiaodan

, p. 8777 - 8782 (2021/11/17)

An efficient approach via catalytic electrophilic thiocarbocyclization of allenes to construct indene-based sulfides with excellent regioselectivities is disclosed. The reactions were carried out at low temperatures by selenide catalysis in the presence o

Cu(I)-catalyzed coupling of diaryldiazomethanes with terminal alkynes: An efficient synthesis of tri-aryl-substituted allenes

Wu, Chenggui,Hu, Fangdong,Liu, Zhenxing,Deng, Guisheng,Ye, Fei,Zhang, Yan,Wang, Jianbo

, p. 9196 - 9201 (2015/11/27)

A highly efficient method for the synthesis of tri-aryl-substituted allenes has been developed through Cu(I)-catalyzed coupling of diaryldiazomethanes with terminal alkynes. The reaction is under mild conditions and uses simple and inexpensive CuI as the catalyst. Mechanistically, the reaction follows a pathway involving Cu(I) carbene migratory insertion.

Coupling of n-tosylhydrazones with terminal alkynes catalyzed by copper(i): Synthesis of trisubstituted allenes

Xiao, Qing,Xia, Ying,Li, Huan,Zhang, Yan,Wang, Jianbo

experimental part, p. 1114 - 1117 (2011/04/16)

The easy way to allenes: An operationally simple reaction under mild conditions has led to the direct formation of trisubstituted allenes (see scheme; Ts=4-toluenesulfonyl). An unprecedented copper-carbene migratory insertion process seems to take place,

FORMATION OF ALLENYL CATIONS BY PHOTOLYSIS OF TRIARYLCHLOROALLENES

Kitamura, Tsugio,Miyake, Sumiya,Kobayashi, Shinjiro,Taniguchi, Hiroshi

, p. 929 - 930 (2007/10/02)

Irradiation of triarylchloroallenes in methanol afforded 1,3,3-triaryl-3-methoxypropynes, suggesting the intervention of triarylallenyl cations.Irradiation of triphenylchloroallene in ethanol and 2-propanol gave the similar results but the irradiation in

CUMULENE PHOTOCHEMISTRY: PHENYL AND HYDROGEN MIGRATION IN PHENYLALLENE PHOTOREACTIONS

Klett, Michael W.,Johnson, Richard P.

, p. 2523 - 2526 (2007/10/02)

Photoreactions of tetra- and triphenylallene and 1,3,3-triphenylcyclopropane in hydrocarbon solvents are reported.Intermediacy of vinylcarbenes is supported by independent generation experiments.

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