2-(3-Bromophenyl)furan is an organic compound characterized by the presence of a furan ring substituted with a bromophenyl group. The furan moiety is a five-membered aromatic ring containing four carbon atoms and one oxygen atom, contributing to its reactivity and stability. The bromophenyl substituent, specifically located at the 3-position of the phenyl ring, introduces both steric and electronic effects that can influence the compound's chemical behavior. This compound is typically a pale yellow to brown solid, and it is soluble in organic solvents such as dichloromethane and ethanol, but less soluble in water. Its properties make it of interest in various fields, including organic synthesis and medicinal chemistry, where it may serve as a building block for more complex molecules or as a potential pharmacophore. Additionally, the presence of the bromine atom can facilitate further chemical modifications, such as nucleophilic substitutions or coupling reactions, enhancing its utility in synthetic applications. Safety data should be consulted, as halogenated compounds can exhibit varying degrees of toxicity and environmental impact.

2-(3-Bromophenyl)furan

85553-51-1: 2-(3-Bromophenyl)furan is an organic compound characterized by the presence of a furan ring substituted with a bromophenyl group. The furan moiety is a five-membered aromatic ring containing four carbon atoms and one oxygen atom, contributing to its reactivity and stability. The bromophenyl substituent, specifically located at the 3-position of the phenyl ring, introduces both steric and electronic effects that can influence the compound's chemical behavior. This compound is typically a pale yellow to brown solid, and it is soluble in organic solvents such as dichloromethane and ethanol, but less soluble in water. Its properties make it of interest in various fields, including organic synthesis and medicinal chemistry, where it may serve as a building block for more complex molecules or as a potential pharmacophore. Additionally, the presence of the bromine atom can facilitate further chemical modifications, such as nucleophilic substitutions or coupling reactions, enhancing its utility in synthetic applications. Safety data should be consulted, as halogenated compounds can exhibit varying degrees of toxicity and environmental impact.

CAS 85553-51-1

2-(3-Bromophenyl)furan

2-(3-Bromophenyl)furan

Ref: 54-OR9298