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Hexa-1,5-diene-1,1,3,4,6,6-hexaylhexabenzene is a complex organic compound consisting of a hexabenzene core with a hexa-1,5-diene moiety attached to it. The hexabenzene core is a planar, hexagonal arrangement of six benzene rings, while the hexa-1,5-diene moiety is a conjugated diene with alternating double and single bonds. hexa-1,5-diene-1,1,3,4,6,6-hexaylhexabenzene is characterized by its unique structure, which allows for interesting electronic properties and potential applications in materials science and organic chemistry. Due to its large size and complex structure, hexa-1,5-diene-1,1,3,4,6,6-hexaylhexabenzene is a challenging molecule to synthesize and study, but it offers a fascinating insight into the world of organic chemistry and the potential for designing new materials with unique properties.

6817-43-2

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6817-43-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6817-43-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,1 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6817-43:
(6*6)+(5*8)+(4*1)+(3*7)+(2*4)+(1*3)=112
112 % 10 = 2
So 6817-43-2 is a valid CAS Registry Number.

6817-43-2Downstream Products

6817-43-2Relevant academic research and scientific papers

Palladium-Catalyzed Allyl-Allyl Reductive Coupling of Allylamines or Allylic Alcohols with H2as Sole Reductant

Zhou, Xibing,Zhang, Guoying,Huang, Renbin,Huang, Hanmin

supporting information, p. 365 - 369 (2021/01/26)

Catalytic carbon-carbon bond formation building on reductive coupling is a powerful method for the preparation of organic compounds. The identification of environmentally benign reductants is key for establishing an efficient reductive coupling reaction. Herein an efficient strategy enabling H2 as the sole reductant for the palladium-catalyzed allyl-allyl reductive coupling reaction is described. A wide range of allylamines and allylic alcohols as well as allylic ethers proceed smoothly to deliver the C-C coupling products under 1 atm of H2. Kinetic studies suggested that the dinuclear palladium species was involved in the catalytic cycle.

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