alpha-(2-Bromophenyl)benzylamine
≥97%
- Product Code: 56796
CAS:
55095-15-3
| Molecular Weight: | 262.15 g./mol | Molecular Formula: | C₁₃H₁₂BrN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09731160 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Alpha-(2-Bromophenyl)benzylamine is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various pharmacologically active compounds. It serves as a key building block in the development of pharmaceuticals, particularly in the synthesis of molecules with potential therapeutic applications. The bromine atom on the phenyl ring makes it a valuable substrate for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of complex structures. Additionally, its amine group allows for the formation of amides, Schiff bases, or other derivatives, expanding its utility in medicinal chemistry. This compound is also explored in the design of ligands for catalysis and in the study of receptor-binding interactions, contributing to advancements in drug discovery and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | Ft244,162.84 |
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| 25.000 | 10-20 days | Ft720,076.73 |
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alpha-(2-Bromophenyl)benzylamine
Alpha-(2-Bromophenyl)benzylamine is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various pharmacologically active compounds. It serves as a key building block in the development of pharmaceuticals, particularly in the synthesis of molecules with potential therapeutic applications. The bromine atom on the phenyl ring makes it a valuable substrate for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of complex structures. Additionally, its amine group allows for the formation of amides, Schiff bases, or other derivatives, expanding its utility in medicinal chemistry. This compound is also explored in the design of ligands for catalysis and in the study of receptor-binding interactions, contributing to advancements in drug discovery and material science.
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