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Anthracene, 9-(3-fluorophenyl)-, also known as 9-(3-fluorophenyl)anthracene, is an organic compound with the chemical formula C20H13F. It is a derivative of anthracene, a polycyclic aromatic hydrocarbon, with a fluorophenyl group attached at the 9th position. Anthracene, 9-(3-fluorophenyl)- is characterized by its planar structure and strong fluorescence properties, making it useful in various applications such as organic light-emitting diodes (OLEDs), sensors, and as a building block in the synthesis of more complex molecules. Due to its potential environmental and health impacts, it is important to handle and dispose of this chemical responsibly, following proper safety guidelines.

386-20-9

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386-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 386-20-9 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 386-20:
(5*3)+(4*8)+(3*6)+(2*2)+(1*0)=69
69 % 10 = 9
So 386-20-9 is a valid CAS Registry Number.

386-20-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(3-fluorophenyl)anthracene

1.2 Other means of identification

Product number -
Other names Anthracene,9-(3-fluorophenyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:386-20-9 SDS

386-20-9Downstream Products

386-20-9Relevant 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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