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3,6-Diphenyl-octa-2ξ,6ξ-diene is a chemical compound characterized by its unique structure, which consists of an octadiene backbone with two phenyl groups attached at the 3 and 6 positions. This organic molecule is a conjugated diene, meaning it has two carbon-carbon double bonds separated by a single carbon-carbon single bond, which allows for the delocalization of electrons and contributes to its chemical properties. The presence of phenyl groups enhances its aromatic character and stability. 3,6-diphenyl-octa-2ξ,6ξ-diene is of interest in organic chemistry and materials science due to its potential applications in the synthesis of various polymers and pharmaceuticals, as well as its role as an intermediate in the production of other complex organic molecules.

1772-26-5

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1772-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1772-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1772-26:
(6*1)+(5*7)+(4*7)+(3*2)+(2*2)+(1*6)=85
85 % 10 = 5
So 1772-26-5 is a valid CAS Registry Number.

1772-26-5Relevant academic research and scientific papers

Synthesis of 2,5-Diaryl-1,5-dienes from Allylic Bromides Using Visible-Light Photoredox Catalysis

Pratsch, Gerald,Overman, Larry E.

, p. 11388 - 11397 (2015/12/01)

Visible-light photoreductive coupling of 2-arylallyl bromides in the presence of the photocatalyst Ru(bpy)3(PF6)2, a Hantzsch ester, and i-Pr2NEt gives 2,5-diaryl-1,5-dienes in high yield. This method avoids the use of stoichiometric metal reductants and is compatible with the presence of halogen, alkyl, electron-donating, and electron-withdrawing substituents on the aromatic ring.

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