Nom du produit:((2-bromoethoxy)methyl)benzene

IUPAC Name:[(2-bromoethoxy)methyl]benzene

CAS:1462-37-9
Formule moléculaire:C9H11BrO
Pureté:95%+
Numéro de catalogue:CM147865
Poids moléculaire:215.09

Unité d'emballage Stock disponible Prix($) Quantité
CM147865-100g in stock źƞ

Pour une utilisation en R&D uniquement..

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Détails du produit

N° CAS:1462-37-9
Formule moléculaire:C9H11BrO
Point de fusion:-
Code SMILES:BrCCOCC1=CC=CC=C1
Densité:
Numéro de catalogue:CM147865
Poids moléculaire:215.09
Point d'ébullition:258.6°C at 760 mmHg
N° Mdl:MFCD01321307
Stockage:Store at room temperature.

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Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

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Product Overview ((2-bromoethoxy)methyl)benzene, also known as BEMB, is a highly versatile organic compound with a wide range of applications in organic synthesis and scientific research. BEMB is an aromatic compound consisting of a benzene ring with a bromoethoxy substituent, and is used as a building block in organic synthesis for the production of various other compounds. It is also used in scientific research, as it has been found to possess a range of biological activities, including anti-inflammatory, anti-cancer, and antioxidant effects.
Synthesis and Application ((2-Bromoethoxy)methyl)benzene is synthesized from a variety of starting materials, including benzene, ethylene oxide, and bromine. The most commonly used method for the synthesis of ((2-Bromoethoxy)methyl)benzene is the Williamson ether synthesis, which involves the reaction of an alkyl halide with an alkyl alcohol in the presence of a base. The reaction of benzene with ethylene oxide in the presence of a base produces ethylene glycol, which is then reacted with bromine to produce ((2-Bromoethoxy)methyl)benzene. Other methods for the synthesis of ((2-Bromoethoxy)methyl)benzene include the formation of an ester from an alkyl halide and an alcohol, followed by reaction with bromine to form ((2-Bromoethoxy)methyl)benzene. ((2-Bromoethoxy)methyl)benzene has a wide range of applications in scientific research, including in vivo and in vitro studies. In vivo studies involve the use of ((2-Bromoethoxy)methyl)benzene in animals, while in vitro studies involve the use of ((2-Bromoethoxy)methyl)benzene in cell cultures or other laboratory experiments. ((2-Bromoethoxy)methyl)benzene has been found to possess a range of biological activities, including anti-inflammatory, anti-cancer, and antioxidant effects.
Future Directions The use of ((2-Bromoethoxy)methyl)benzene in scientific research is a rapidly growing field, and there are many potential future directions for further research. These include the development of new synthesis methods for ((2-Bromoethoxy)methyl)benzene, the investigation of its potential therapeutic applications, and the exploration of its potential toxicological effects. In addition, further research into the mechanism of action of ((2-Bromoethoxy)methyl)benzene, and its biochemical and physiological effects, will also be important for the development of new therapeutic applications. Finally, further research into the pharmacodynamics of ((2-Bromoethoxy)methyl)benzene, and its advantages and limitations for laboratory experiments, will also be necessary for the development of new and improved laboratory protocols.