5732-17-2 Usage
Uses
Used in Organic Synthesis:
2,4,6-Triphenylbenzoic acid is used as a building block in organic synthesis for the creation of complex organic molecules. Its aromatic structure and solubility in organic solvents make it a versatile component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Materials Science:
In the field of materials science, 2,4,6-triphenylbenzoic acid is employed as a precursor for the development of novel materials with specific properties. Its aromatic nature and structural features contribute to the formation of materials with potential applications in areas such as electronics, optoelectronics, and polymer science.
Used in Pharmaceutical Research:
2,4,6-Triphenylbenzoic acid is utilized as a starting material in pharmaceutical research for the discovery and development of new drugs. Its chemical structure can be modified to create compounds with potential therapeutic effects, making it a valuable asset in the search for innovative treatments for various diseases.
Used in Chemical Industry:
2,4,6-Triphenylbenzoic acid is used as a precursor in the chemical industry for the preparation of other organic compounds. Its reactivity and structural characteristics allow for the synthesis of a wide range of products, including dyes, pigments, and other specialty chemicals that are used in various industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5732-17-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,3 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5732-17:
(6*5)+(5*7)+(4*3)+(3*2)+(2*1)+(1*7)=92
92 % 10 = 2
So 5732-17-2 is a valid CAS Registry Number.
5732-17-2Relevant articles and documents
Flexible coordination of the carboxylate ligand in tin(II) amides and a 1,3-diaza-2,4-distannacyclobutanediyl
Dickie, Diane A.,Lee, Peter T.K.,Labeodan, Ojisamola A.,Schatte, Gabriele,Weinberg, Noham,Lewis, Andrew R.,Bernard, Guy M.,Wasylishen, Roderick E.,Clyburne, Jason A.C.
, p. 2862 - 2869 (2008/02/10)
A series of tin(ii) amido complexes possessing m-terphenyl carboxylate ligands have been prepared. These complexes, namely [(Me3Si) 2NSn(-O2CC6H2Ph3)] 2, [(Me3Si)2NSn(-O2CC 6H3Mes2)]2, and [(Me 3Si)2NSn(-O2CC6H2Mes 2Me)]2 [Mes = 2,4,6-trimethylphenyl], are the first structurally characterized examples of tin(ii) carboxylate complexes exhibiting discrete Sn2O4C2 heterocyclic cores. Initial reactivity studies led to the isolation of a 1,3-diaza-2,4- distannacyclobutanediyl, [(Mes2C6H3CO 2)Sn(-NSiMe3)]2. This molecule possesses a Sn2N2 heterocyclic core and it was crystallised as both the CH2Cl2 and Et2O solvates. Although the tin atoms in this molecule have a formal oxidation state of 3+, preliminary computational studies on this molecule suggest that it is best described as a ground state singlet. Finally, the X-ray crystal structure of (CH 2Cl)(Cl)Sn[N(SiMe3)2]2, the product of oxidative addition of CH2Cl2 to Sn[N(SiMe 3)2]2, is also presented herein. The Royal Society of Chemistry.
RHODIUM(II)2,4,6-TRIARYLBENZOATES: IMPROVED CATALYSTS FOR THE SYN CYCLOPROPANATION OF Z-OLEFINS
Callot, H. J.,Metz, F.
, p. 4495 - 4502 (2007/10/02)
The stereochemical course of the cyclopropanation of Z-olefins by ethyl diazoacetate in the presence of various binuclear rhodium(II)carboxylates was studied.The highest syn/anti ratio (up to 3) was obtained using Rh2(O2CR)3(O2CR') where R = 2,4,6-triarylphenyl and R' = CH3 or CF3.
