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ethyl (2E,4Z)-4,5-diphenylpenta-2,4-dienoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134641-26-2

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134641-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134641-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,6,4 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 134641-26:
(8*1)+(7*3)+(6*4)+(5*6)+(4*4)+(3*1)+(2*2)+(1*6)=112
112 % 10 = 2
So 134641-26-2 is a valid CAS Registry Number.

134641-26-2Relevant academic research and scientific papers

Exploring bis(cyclometalated) ruthenium(II) complexes as active catalyst precursors: Room-temperature alkene-alkyne coupling for 1,3-diene synthesis

Zhang, Jing,Ugrinov, Angel,Zhang, Yong,Zhao, Pinjing

supporting information, p. 8437 - 8440 (2014/08/18)

Described is the development of a new class of bis(cyclometalated) ruthenium(II) catalyst precursors for C-C coupling reactions between alkene and alkyne substrates. The complex [(cod)Ru(3-methallyl)2] reacts with benzophenone imine or benzophe

Substituent effects on the iodine-catalyzed thermal cyclization of 3,4-diphenylbuta-1,3-dienyl isocyanates: Mechanistic studies

Chuang, Ta-Hsien,Chang, Wei-Yu,Li, Chien-Fu,Wen, Yu-Chia,Tsai, Chia-Chen

experimental part, p. 9678 - 9686 (2012/01/05)

The thermal cyclization of 3,4-diphenylbuta-1,3-dienyl isocyanates 1, generated in situ from the corresponding azides, was investigated using iodine as a catalyst. Diphenylpyridinones 2, phenylnaphthalenes 3, and indenes 4 were produced via intramolecular ring closure. The nature of the substituents on the phenyl rings was found to be crucial to the distribution of cyclized products 2 - 4. The mechanism of the reaction is also discussed.

Ruthenium/halide catalytic system for C-C bond forming reaction between alkynes and unsaturated carbonyl compounds

Nishimura, Takahiro,Washitake, Yosuke,Uemura, Sakae

, p. 2563 - 2571 (2008/09/19)

A ruthenium complex [triruthenium dodecacarbonyl, Ru3(CO) 12] in the presence of bis(triphenylphosphine)iminium chloride ([PPN]Cl) catalyzes the conjugate addition of terminal alkynes to alkyl acrylates to give high yields of γ,δ-alkynyl esters. On the other hand, the linear codimerization reaction of terminal alkynes with alkyl acrylates proceeds in the presence of a catalytic amount of Ru 3(CO)12 and lithium iodide to give the corresponding conjugate dienes. These two different types of catalytic carbon-carbon bond forming reactions are controlled only by the nature of halide ions, either a chloride or an iodide, with other conditions being kept almost the same.

Ruthenium Complex-catalysed Highly Selective Codimerisation of Acetylenes and Alkenes

Mitsudo, Take-aki,Zhang, Shi-Wei,Nagao, Masaki,Watanabe, Yoshihisa

, p. 598 - 599 (2007/10/02)

2,4-Dienes are prepared in high yields with high regioselectivity by the codimerisation of acetylenes and alkenes in the presence of a catalytic amount of Ru(cod)(cot) at 80 deg C; cod = cycloocta-1,5-diene, cot = cycloocta-1,3,5-triene.

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