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2-Butene-1,4-diol, 1,1,4,4-tetraphenyl-, (E)- is a complex organic compound with the molecular formula C26H24O2. It is characterized by its unique structure, featuring a butene-1,4-diol backbone with four phenyl groups attached to the 1, 1, 4, and 4 positions. The "(E)-" notation indicates that the compound has a specific geometric isomerism, with the phenyl groups on the double bond being on the same side of the molecule. 2-Butene-1,4-diol, 1,1,4,4-tetraphenyl-, (E)- is known for its potential applications in various chemical and pharmaceutical industries, particularly in the synthesis of other complex organic molecules and as a precursor in the production of certain pharmaceuticals. Its unique structure and properties make it an interesting subject for research in organic chemistry.

59856-52-9

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59856-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59856-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,5 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59856-52:
(7*5)+(6*9)+(5*8)+(4*5)+(3*6)+(2*5)+(1*2)=179
179 % 10 = 9
So 59856-52-9 is a valid CAS Registry Number.

59856-52-9Relevant academic research and scientific papers

The Pyrolyses of 1,1,4,4-Tetraphenyl-1,4-butanediol and 1,1,4,4-Tetraphenyl-2-butene-1,4-diol Derivatives. Decomposition Reactions to Form Olefins via the Elimination of Two Mole Equivalents of the Hydroxydiphenylmethyl Radical

Saito, Katsuhiro,Horie, Yoichi,Mukai, Toshio,Toda, Takashi

, p. 3118 - 3124 (2007/10/02)

The pyrolysis of 1,1,2,4,4-pentaphenyl-1,4-butandiol, trans-1,2-bis(hydroxydiphenylmethyl)hexane, trans-1,2-bis(hydroxydiphenylmethyl)indan, and cis-endo- and trans-1,2-bis(hydroxydiphenylmethyl)bicycloheptane gave styrene, cyclohexene, indene, and norbornene respectively, accompanied by benzophenone and benzhydrol.The pyrolysis of trans-1,2-bis(hydroxydiphenylmethyl)spironona-4,6,8-triene afforded indene via rearrangement to form trans-1,2-bis(hydroxydiphenylmethyl)indan.The pyrolysis of cis-1,1,4,4-tetraphenyl-2-butene-1,4-diol afforded 2,2,5,5-tetraphenyl-2,5-dihydrofuran.On the other hand, trans-1,1,4,4-tetraphenyl-2- butene-1,4-diol afforded 1,2,4,4-tetraphenyl-3-buten-1-one.The mechanisms of these decomposition reactions are discussed.

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