3-Bromoanisole

CAS : 2398-37-0

Ref. 3D-FB05066

Informations sur le produit

• Nom: 3-Bromoanisole
• Synonymes: 1-Bromo-3-Methoxy-Benzen, 1-Bromo-3-methoxybenzene, 3-Bromanisol, 3-Bromo Anisol, 3-Bromo Anisole For Synthesis, 3-Bromo anisole, 3-Bromoanisol, 3-Bromobenzene methyl ether, 3-Methoxy-1-bromobenzene, 3-Methoxybromobenzene, 3-Methoxyphenyl bromide, 5-Bromoanisole, Anisole, 3-Bromo-, Anisole, m-bromo-, Benzene, 1-bromo-3-methoxy-, Bromoanisole(3-), M-Bromoanisole, Meta Bromo Anisole, Nsc 82293, Timtec-Bb Sbb007886, m-Anisyl bromide, m-BROMO ANISOLE, m-Bromoanisoles, m-Bromomethoxybenzene, m-Bromophenyl methyl ethe, m-Bromophenyl methyl ether, m-Bromophenylmethylether, m-Methoxybromobenzene, m-Methoxyphenyl bromide

Description

3-Bromoanisole is a chemical compound that is used as a solvent for organic reactions. It is typically used in Suzuki coupling reactions, which are employed to form carbon-carbon bonds between two organic molecules. 3-Bromoanisole has been shown to be more reactive than 2-bromoanisole and reacts with hydrogen chloride in hydrochloric acid to form the corresponding bromoalkane. 3-Bromoanisole also participates in molecular interactions by forming steric interactions with other molecules or atoms. This can be seen through molecular modeling studies, where it was observed that 3-bromoanisole interacts with the methoxy group of an adjacent molecule. The sterics of this interaction are illustrated by the increased distance between the two molecules when compared with those without bromoalkanes present.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 187.03 g/mol
• Formule: C₇H₇BrO
• Degré de pureté: Min. 95%
• Couleur/Forme: Powder
• InChI: InChI=1S/C7H7BrO/c1-9-7-4-2-3-6(8)5-7/h2-5H,1H3
• Code InChI: InChIKey=PLDWAJLZAAHOGG-UHFFFAOYSA-N
• SMILES: COc1cccc(Br)c1