605-05-0 Usage
Description
(9-Phenanthryl)phenylmethane, also known as 9-phenylphenanthrene, is a chemical compound with the molecular formula C20H16. It features a phenanthrene ring with a phenyl group attached at the 9-position, which endows it with unique structural and electronic properties. (9-Phenanthryl)phenylmethane is recognized for its significance in various scientific and technological domains due to its versatile characteristics and broad potential applications.
Uses
Used in Organic Chemistry:
(9-Phenanthryl)phenylmethane is utilized as a fundamental building block in the synthesis of a wide array of organic compounds. Its strategic position in the field of organic chemistry is attributed to its ability to facilitate the creation of complex molecular structures.
Used in Biological and Medicinal Research:
(9-Phenanthryl)phenylmethane serves as a fluorescent probe in biological and medicinal research. The distinctive structural and electronic attributes of (9-Phenanthryl)phenylmethane make it a valuable tool for investigating various biological processes and interactions at the molecular level.
Used in Materials Science:
(9-Phenanthryl)phenylmethane holds promise in the realm of materials science, particularly concerning the advancement of organic electronics and optoelectronic devices. Its unique properties render it a potential candidate for enhancing the performance and functionality of these cutting-edge technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 605-05-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 605-05:
(5*6)+(4*0)+(3*5)+(2*0)+(1*5)=50
50 % 10 = 0
So 605-05-0 is a valid CAS Registry Number.
InChI:InChI=1/C21H16/c1-2-8-16(9-3-1)14-18-15-17-10-4-5-11-19(17)21-13-7-6-12-20(18)21/h1-13,15H,14H2
605-05-0Relevant articles and documents
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Bonner,Mosher
, p. 4249 (1948)
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Gold(I)-catalyzed Benzylation of (Hetero)aryl Boronic Acids with (Hetero)benzyl Bromides by the Strategy of a SN2-type Reaction
Zang, Wenqing,Wei, Yin,Shi, Min
supporting information, p. 2791 - 2795 (2018/09/20)
Herein, the first example of gold-catalyzed benzylation of (hetero)aryl boronic acids with (hetero)benzyl bromides to give the corresponding cross-coupling products in moderate to good yields is reported. The reaction proceeds through a possible intermolecular SN2-type reaction pathway to give a wide variety of di(hetero)arylmethanes as the desired products. An intriguing reaction mechanism has been proposed on the basis of control experiments, 31P-NMR spectroscopic detection and DFT calculations.
Pd(II)-NHDC-Functionalized UiO-67 Type MOF for Catalyzing Heck Cross-Coupling and Intermolecular Benzyne-Benzyne-Alkene Insertion Reactions
Wei, Yong-Liang,Li, Yue,Chen, Yun-Qi,Dong, Ying,Yao, Jia-Jia,Han, Xin-Yue,Dong, Yu-Bin
, p. 4379 - 4386 (2018/04/25)
A novel palladium N-heterocyclic bis-carbene dicarboxylate ligand (Pd-NHDC-H2L) was successfully synthesized. In addition, an Pd-NHDC-containing UiO-67 type MOF (UiO-67-Pd-NHDC) was prepared on the basis of a size-matched ligand mixture of biphenyl-4,4′-dicarboxylic acid/Pd-NHDC-H2L (9/1) and ZrCl4 under solvothermal conditions. The obtained UiO-67-Pd-NHC MOF can be a highly heterogeneous catalyst to promote Heck cross-coupling and intermolecular benzyne-benzyne-alkene insertion reactions.
