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19462-79-4

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19462-79-4 Usage

General Description

4-Bromophenanthrene is a chemical compound consisting of a bromine atom attached to a phenanthrene molecule. It is categorized as a halogenated polycyclic aromatic hydrocarbon (PAH) and is a derivative of phenanthrene, which is a constituent of coal tar. 4-Bromophenanthrene is used primarily in research and laboratory settings, particularly for studying the environmental and health impacts of PAHs. Its properties and potential effects are of interest due to the widespread presence of PAHs in the environment as pollutants from combustion processes, and their potential carcinogenic and toxic effects. Additionally, 4-Bromophenanthrene is also used in the synthesis of other organic compounds and can be a useful intermediate in the production of various chemicals. However, due to its potential hazards, proper precautions and safety measures should be taken when handling and using 4-Bromophenanthrene.

Check Digit Verification of cas no

The CAS Registry Mumber 19462-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,6 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19462-79:
(7*1)+(6*9)+(5*4)+(4*6)+(3*2)+(2*7)+(1*9)=134
134 % 10 = 4
So 19462-79-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H9Br/c15-13-7-3-5-11-9-8-10-4-1-2-6-12(10)14(11)13/h1-9H

19462-79-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromophenanthrene

1.2 Other means of identification

Product number -
Other names 4-Bromphenanthren

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:19462-79-4 SDS

19462-79-4Downstream Products

19462-79-4Relevant articles and documents

Novel compound and organic light emitting device comprising the same

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Paragraph 0366; 0371, (2021/11/30)

The present invention provides a novel compound and an organic light emitting device using the same.

Organic compound, electronic component comprising same and electronic device

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Paragraph 0155; 0169-0171; 0172-0174, (2021/02/10)

The invention relates to an organic compound, an electronic component comprising the same and an electronic device, and belongs to the technical field of organic electroluminescence. According to theorganic electroluminescent material disclosed by the invention, the molecule contains an adamantane-phenanthrene structure, so that the electron density of a conjugated system is increased, and the hole conduction efficiency of the organic compound is further improved. When the organic electroluminescent material provided by the invention is applied to a functional layer of an organic electroluminescent device, the performance of the organic electroluminescent device can be improved.

Alumina-Mediated π-Activation of Alkynes

Akhmetov, Vladimir,Amsharov, Konstantin,Feofanov, Mikhail,Sharapa, Dmitry I.

, p. 15420 - 15426 (2021/09/30)

The ability to induce powerful atom-economic transformation of alkynes is the key feature of carbophilic π-Lewis acids such as gold- and platinum-based catalysts. The unique catalytic activity of these compounds in electrophilic activations of alkynes is explained through relativistic effects, enabling efficient orbital overlapping with π-systems. For this reason, it is believed that noble metals are indispensable components in the catalysis of such reactions. In this study, we report that thermally activated γ-Al2O3activates enynes, diynes, and arene-ynes in a manner enabling reactions that were typically assigned to the softest π-Lewis acids, while some were known to be triggered exclusively by gold catalysts. We demonstrate the scope of these transformations and suggest a qualitative explanation of this phenomenon based on the Dewar-Chatt-Duncanson model confirmed by density functional theory calculations.

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