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2,2',6,6'-Tetraphenyl-4,4'-dioxo-2,2'-bi(1,3-dioxenyl) is a complex organic compound characterized by its unique molecular structure. It features two 1,3-dioxenyl rings, which are connected through a central biphenyl core. The compound is adorned with four phenyl groups, two at each end of the biphenyl, enhancing its stability and potentially influencing its chemical properties. This molecule is known for its rigid structure and is often studied for its electronic and optical characteristics, which can be useful in the development of materials for various applications, including electronics and photonics. The compound's specific arrangement of atoms and the presence of oxygen atoms in the dioxenyl rings contribute to its reactivity and potential uses in chemical research and industry.

77092-37-6

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77092-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77092-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,9 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77092-37:
(7*7)+(6*7)+(5*0)+(4*9)+(3*2)+(2*3)+(1*7)=146
146 % 10 = 6
So 77092-37-6 is a valid CAS Registry Number.

77092-37-6Downstream Products

77092-37-6Relevant academic research and scientific papers

CHEMISTRY OF OXALYL DERIVATIVES OF METHYL KETONES. XXIII. REACTION OF 5-ARYL-2,3-DIHYDROFURAN-2,3-DIONES WITH ALDEHYDES AND KETONES

Andreichikov, Yu. S.,Gein, L. F.,Plakhina, G. D.

, p. 1995 - 1998 (2007/10/02)

5-Aryl-2,3-dihydrofuran-2,3-diones react with aldehydes, ketones, and α-ketoesters to form 2,2,5,6-tetrasubstituted 1,3-dioxen-4-ones.The reaction of 5-aryl-2,3-dihydrofuran-2,3-diones with α-diketones occurs either at one carbonyl group of the α-ketone to form 2,6-disubstituted 1,3-dioxen-4-ones or at both carbonyl groups to form 2,2',6,6'-tetrasubstituted 4,4'-dioxo-2,2'-bi(1,3-dioxenyls).

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