23879-81-4 Usage
Description
1,3,5-Triphenoxybenzene is an aromatic organic compound that consists of a benzene ring with three phenoxy (C6H5O) groups attached at positions 1, 3, and 5. It is a white solid with a molecular formula C24H18O3 and a molecular weight of 354.39 g/mol.
Used in Academic Research and Chemical Synthesis:
1,3,5-Triphenoxybenzene is used as a building block for creating other organic compounds, serving as a key component in the synthesis of various organic molecules.
Used in Organic Electronic Devices:
1,3,5-Triphenoxybenzene is used as a precursor for the synthesis of novel materials with interesting optical and electronic properties, making it a valuable component in the development of advanced electronic devices.
Used in Supramolecular Chemistry and Crystal Engineering:
1,3,5-Triphenoxybenzene is used as a structural component in supramolecular chemistry and crystal engineering due to its rigid and planar molecular structure, which allows for the creation of complex and functional materials.
Check Digit Verification of cas no
The CAS Registry Mumber 23879-81-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,7 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23879-81:
(7*2)+(6*3)+(5*8)+(4*7)+(3*9)+(2*8)+(1*1)=144
144 % 10 = 4
So 23879-81-4 is a valid CAS Registry Number.
23879-81-4Relevant articles and documents
Efficient Ni-catalyzed conversion of phenols protected with 2,4,6-trichloro-1,3,5-triazine (TCT) to olefins
Etemadi-Davan,Iranpoor
supporting information, p. 12794 - 12797 (2017/12/06)
An efficient Ni(COD)2/dppf catalyzed olefination of Ar-O-TCT as synthetic equivalents of aryl halides is described. Activation of C-O bonds in phenols as readily available compounds was achieved with 2,4,6-trichloro-1,3,5-triazine (TCT). This method provides practical access to 1,2-disubstituted olefins in high yields and high functional group compatibility.
Replacement of the nitro groups in 1,3,5-trinitrobenzene through the action of phenols; a general method for preparation of 3,5-dinitrophenyl aryl ethers and 5-nitroresorcinol diaryl ethers
Shevelev, S. A.,Dutov, M. D.,Vatsadze, I. A.,Serushkina, O. V.,Korolev, M. A.,Rusanov, A. L.
, p. 384 - 385 (2007/10/02)
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