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9-(3-(trifluoromethyl)phenyl)anthracene is an organic compound characterized by its unique molecular structure, which consists of an anthracene core with a trifluoromethyl-substituted phenyl group attached at the 9th position. 9-(3-(trifluoromethyl)phenyl)anthracene is known for its potential applications in various fields, including materials science and pharmaceuticals, due to its specific electronic and steric properties. The trifluoromethyl group imparts a significant electron-withdrawing effect, which can influence the compound's reactivity and stability. Additionally, the presence of this functional group can lead to unique interactions with other molecules, making it a subject of interest in chemical research and development.

386-21-0

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386-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 386-21-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 386-21:
(5*3)+(4*8)+(3*6)+(2*2)+(1*1)=70
70 % 10 = 0
So 386-21-0 is a valid CAS Registry Number.

386-21-0Downstream Products

386-21-0Relevant academic research and scientific papers

Chromium- and Cobalt-Catalyzed, Regiocontrolled Hydrogenation of Polycyclic Aromatic Hydrocarbons: A Combined Experimental and Theoretical Study

Han, Bo,Ma, Pengchen,Cong, Xuefeng,Chen, Hui,Zeng, Xiaoming

supporting information, p. 9018 - 9026 (2019/06/13)

Polycyclic aromatic hydrocarbons are difficult substrates for hydrogenation because of the thermodynamic stability caused by aromaticity. We report here the first chromium- and cobalt-catalyzed, regiocontrolled hydrogenation of polycyclic aromatic hydrocarbons at ambient temperature. These reactions were promoted by low-cost chromium or cobalt salts combined with diimino/carbene ligand and methylmagnesium bromide and are characterized by high regioselectivity and expanded substrate scope that includes tetracene, tetraphene, pentacene, and perylene, which have rarely been reduced. The approach provides a cost-effective catalytic protocol for hydrogenation, is scalable, and can be utilized in the synthesis of tetrabromo- and carboxyl-substituted motifs through functionalization of the hydrogenation product. The systematic theoretical mechanistic modelings suggest that low-valent Cr and Co monohydride species, most likely from zerovalent transition metals, are capable of mediating these hydrogenations of fused PAHs.

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