1094477-13-0 | 4-(3-bromophenyl)oxan-4-amine

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Description

• Catalog Number: AV55632
• Chemical Name: 4-(3-bromophenyl)oxan-4-amine
• CAS Number: 1094477-13-0
• Molecular Formula: C11H14BrNO
• Molecular Weight: 256.139
• MDL Number: MFCD11642707
• SMILES: Brc1cccc(c1)C1(N)CCOCC1

Upstream Synthesis Route

4-(3-Bromophenyl)tetrahydro-2H-pyran-4-amine is a versatile compound widely used in various chemical synthesis processes. In organic chemistry, this compound serves as a key building block for the synthesis of complex molecules due to its unique structure and reactivity. Its primary application lies in the formation of heterocyclic compounds, which are essential in the development of pharmaceuticals, agrochemicals, and materials science.One of the crucial roles of 4-(3-Bromophenyl)tetrahydro-2H-pyran-4-amine in chemical synthesis is its participation in nucleophilic substitution reactions. The bromine atom attached to the phenyl ring provides a site for substitution, enabling the introduction of different functional groups. This compound can undergo various transformations, such as Suzuki coupling, Buchwald-Hartwig amination, and Heck reaction, leading to the creation of diverse chemical structures with desired properties.Additionally, 4-(3-Bromophenyl)tetrahydro-2H-pyran-4-amine finds application in cascade reactions, where multiple bond-forming events occur in a single synthetic step. This compound's ability to participate in sequential transformations enhances the efficiency of complex molecule synthesis by reducing the number of required steps and overall reaction time.Furthermore, the presence of the tetrahydro-2H-pyran moiety in 4-(3-Bromophenyl)tetrahydro-2H-pyran-4-amine enhances its stability and solubility, making it a valuable reagent for various synthetic methodologies. Its compatibility with different reaction conditions and its capacity to facilitate the creation of diverse chemical scaffolds highlight its significance in modern organic synthesis and drug discovery efforts.