25871-69-6 Usage
Description
1,3,5-TRIBENZOYLBENZENE is an organic compound that serves as a tritopic ligand in the synthesis and characterization of coordination polymers. It is a versatile molecule with potential applications in various fields due to its unique structure and properties.
Uses
Used in Chemical Synthesis:
1,3,5-TRIBENZOYLBENZENE is used as a tritopic ligand for the synthesis and characterization of three new coordination polymers. Its unique structure allows for the formation of complex and diverse coordination polymers, which can have various applications in different industries.
Used in Pharmaceutical Industry:
1,3,5-TRIBENZOYLBENZENE, as a ligand, can be employed in the development of new pharmaceutical compounds. The coordination polymers synthesized using this ligand may exhibit specific biological activities or properties that can be utilized in the design of novel drugs for various therapeutic applications.
Used in Materials Science:
The coordination polymers formed using 1,3,5-TRIBENZOYLBENZENE as a ligand may have unique properties that can be exploited in the development of new materials for various applications, such as in electronics, sensors, or energy storage devices.
Used in Research and Development:
1,3,5-TRIBENZOYLBENZENE can be used as a starting point for further research and development in the field of coordination chemistry. The study of the properties and applications of the coordination polymers synthesized using this ligand can lead to the discovery of new compounds and materials with potential uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 25871-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,7 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25871-69:
(7*2)+(6*5)+(5*8)+(4*7)+(3*1)+(2*6)+(1*9)=136
136 % 10 = 6
So 25871-69-6 is a valid CAS Registry Number.
InChI:InChI=1/C27H18O3/c28-25(19-10-4-1-5-11-19)22-16-23(26(29)20-12-6-2-7-13-20)18-24(17-22)27(30)21-14-8-3-9-15-21/h1-18H
25871-69-6Relevant articles and documents
Convenient access to 1,3,5-triaroylbenzenes
Joseph, Delphine,Jankowski, Raphael,Prim, Damien,Mahuteau, Jacqueline,Chiaroni, Angèle
, p. 8051 - 8054 (2002)
The unusual transformation of β-aryl-β-haloacroleins into valuable triaroylbenzenes is reported by the first time. The convenient sequence takes advantage on the one step access to triaroylbenzenes. This work establishes that the presence of amine is required for the trimerization procedure since it is involved in the formation of iminium-enamine intermediate A.
Aromatic ketone compound and organic light-emitting device thereof
-
, (2020/03/12)
The invention provides an aromatic ketone compound and an organic light-emitting device. thereof, wherein the aromatic ketone compound has the structure (I) shown, in a formula shown in the description . X1 And X2 The lines are the s
Microporous, tetraarylethylene-based polymer networks generated in a reductive polyolefination process
Preis,Dong,Brunklaus,Scherf
supporting information, p. 1582 - 1587 (2015/04/27)
Microporous Polymer Networks (MPNs) that contain aggregate-induced emission (AIE) active tetraphenylethylene (TPE) or other tetraarylethylene units have been generated in a reductive polyolefination process starting from four different tris(α,α-dichlorobenzyl)arene derivatives with dicobalt octacarbonyl or chromium(ii)acetate as reductive olefination agents. Microporosity with moderately high BET surface areas up to 500 m2 g-1 could be combined with high solid state photoluminescence quantum yields up to 25.3% for polymer network P4. This unique combination should be promising for applications as optical solid state sensors, especially for MPNs with electron-deficient triazine core units.
