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9-(2-fluorophenyl)anthracene is an organic compound characterized by its unique molecular structure, which consists of an anthracene core with a fluorophenyl group attached at the 9th position. This fluorinated derivative of anthracene exhibits distinct chemical and physical properties due to the presence of the fluorine atom, which influences its reactivity, stability, and electronic properties. The compound is of interest in various fields, including materials science, pharmaceuticals, and chemical research, where its specific characteristics can be exploited for the development of new technologies and applications.

737-24-6

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737-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 737-24-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 737-24:
(5*7)+(4*3)+(3*7)+(2*2)+(1*4)=76
76 % 10 = 6
So 737-24-6 is a valid CAS Registry Number.

737-24-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(2-fluorophenyl)anthracene

1.2 Other means of identification

Product number -
Other names -

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:737-24-6 SDS

737-24-6Downstream Products

737-24-6Relevant 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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