1608-11-3 Usage
Description
(1Z,3Z)-1,2,3,4-Tetraphenyl-1,3-butadiene is an organic compound with the molecular formula C28H22. It is a conjugated polyene, characterized by the presence of two double bonds separated by single bonds. (1Z,3Z)-1,2,3,4-Tetraphenyl-1,3-butadiene is known for its unique structure and reactivity, making it a valuable building block in organic synthesis.
Uses
Used in Organic Synthesis:
(1Z,3Z)-1,2,3,4-Tetraphenyl-1,3-butadiene is used as a building block for the production of various organic compounds. Its unique structure and reactivity allow it to undergo a wide range of chemical reactions, making it a versatile component in the synthesis of complex organic molecules.
Used in Diels-Alder Reactions:
(1Z,3Z)-1,2,3,4-Tetraphenyl-1,3-butadiene is used as a diene in Diels-Alder reactions, a type of [4+2] cycloaddition. This reaction is a powerful method for constructing six-membered rings and is widely used in the synthesis of natural products, pharmaceuticals, and other organic compounds.
Used in Other Cycloadditions:
In addition to Diels-Alder reactions, (1Z,3Z)-1,2,3,4-Tetraphenyl-1,3-butadiene can also participate in other types of cycloadditions. These reactions can lead to the formation of various heterocyclic compounds and other complex molecular structures, further expanding the utility of this compound in organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 1608-11-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1608-11:
(6*1)+(5*6)+(4*0)+(3*8)+(2*1)+(1*1)=63
63 % 10 = 3
So 1608-11-3 is a valid CAS Registry Number.
1608-11-3Relevant articles and documents
Palladium-catalyzed hydrophenylation of alkynes with sodium tetraphenylborate under mild conditions
Zeng, Hanxiang,Hua, Ruimao
, p. 558 - 562 (2008/09/17)
(Chemical Equation Presented) In an aqueous solution of acetic acid, PdCl2(PPh3)2 showed high catalytic activity for the hydrophenylation of both terminal and internal alkynes with sodium tetraphenylborate (NaBPh4) under mild conditions, affording phenyl alkenes in moderate to excellent yields.
