Product Name:2-Bromoanthracene

IUPAC Name:2-bromoanthracene

CAS:7321-27-9
Molecular Formula:C14H9Br
Purity:97%
Catalog Number:CM254793
Molecular Weight:257.13

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CM254793-25g in stock ƄǤ
CM254793-100g in stock NJǵĽ

For R&D use only.

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Product Details

CAS NO:7321-27-9
Molecular Formula:C14H9Br
Melting Point:-
Smiles Code:BrC1=CC=C2C=C3C=CC=CC3=CC2=C1
Density:
Catalog Number:CM254793
Molecular Weight:257.13
Boiling Point:389.7°C at 760 mmHg
MDL No:MFCD07784002
Storage:Store at room temperature.

Category Infos

Anthracenes
Anthracene is a condensed aromatic hydrocarbon containing three rings. The center of the three rings of anthracene is in a straight line, which is the isomer of phenanthrene. The chemical activity of the 9 and 10 positions in the anthracene molecule is relatively high. It is oxidized with nitric acid to generate 9, 10-anthraquinone, which is an important intermediate for the synthesis of anthraquinone dyes. Anthracene can also act as a conjugated diene in a Diels-Alder reaction with maleic anhydride.

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Product Other Information

Product Overview 2-Bromoanthracene (2-BrA) is a polycyclic aromatic hydrocarbon (PAH) that belongs to the anthracene family. 
Physical Properties It is a colorless, crystalline solid.
Chemical Properties 2-Bromoanthracene is a useful compound for laboratory experiments due to its low cost and availability. It is also relatively easy to handle and store, and is not highly toxic. However, it is highly reactive and can undergo unwanted side reactions, and can form hazardous byproducts.
Synthesis and Application It is used in the synthesis of organic molecules, such as dyes, pharmaceuticals, and pesticides. In addition, it is used in the study of chemical reactions, such as the oxidation of aromatic compounds, the formation of polycyclic aromatic hydrocarbons, and the photochemical reactions of aromatic compounds.
Future Directions Future research on 2-Bromoanthracene could focus on the development of new synthetic methods for the preparation of this compound. In addition, further research could be conducted to explore the potential applications of 2-Bromoanthracene in the synthesis of organic molecules and in the study of chemical reactions. Finally, further research could be conducted to investigate the toxic effects of 2-Bromoanthracene on living organisms, and to develop strategies to reduce its toxicity.