N-((5-Bromothiophen-2-Yl)Methyl)Pentan-3-Amine
98%
Reagent
Code: #220133
CAS Number
1019559-37-5
blur_circular Chemical Specifications
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Molecular Information
Weight
262.21 g/mol
Formula
C₁₀H₁₆BrNS
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Storage & Handling
Storage
Room temperature
description Product Description
Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Its structure supports the construction of complex molecules through coupling reactions, making it valuable in drug discovery. The bromine functionality allows for cross-coupling reactions such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. The amine group can be modified or used to enhance solubility and binding properties in biologically active compounds. It is also employed in the synthesis of functionalized heterocyclic compounds, which are common scaffolds in medicinal chemistry.
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