cas 7321-27-9|| where to buy 2-Bromoanthracene

Nom du produit:2-Bromoanthracene

IUPAC Name:2-bromoanthracene

Unité d'emballage	Stock disponible	Prix($)
CM254793-25g	in stock	ƋɅ
CM254793-100g	in stock	ƻǧƱ

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: N° CAS:7321-27-9; Formule moléculaire:C14H9Br; Point de fusion:-; Code SMILES:BrC1=CC=C2C=C3C=CC=CC3=CC2=C1; Densité:

: Numéro de catalogue:CM254793; Poids moléculaire:257.13; Point d'ébullition:389.7°C at 760 mmHg; N° Mdl:MFCD07784002; Stockage:Store at room temperature.

: 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.

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.