N-(4-Bromophenyl)pyrrolidine

98%

Reagent Code: #217233
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CAS Number 22090-26-2

science Other reagents with same CAS 22090-26-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.11 g/mol
Formula C₁₀H₁₂BrN
badge Registry Numbers
MDL Number MFCD04112480
thermostat Physical Properties
Melting Point 107°C
Boiling Point 306.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of bioactive molecules due to the presence of the secondary amine and the electron-deficient aryl bromide, which allows for further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Its structural motif is found in some neuroactive compounds, making it valuable in medicinal chemistry research. Also employed in the synthesis of ligands for catalysis and in the exploration of structure-activity relationships in drug discovery programs.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿280.00
5g
10-20 days ฿1,730.00
1g
10-20 days ฿410.00
N-(4-Bromophenyl)pyrrolidine
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Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of bioactive molecules due to the presence of the secondary amine and the electron-deficient aryl bromide, which allows for further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Its structural motif is found in some neuroactive compounds, making it valuable in medicinal chemistry researc

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of bioactive molecules due to the presence of the secondary amine and the electron-deficient aryl bromide, which allows for further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Its structural motif is found in some neuroactive compounds, making it valuable in medicinal chemistry research. Also employed in the synthesis of ligands for catalysis and in the exploration of structure-activity relationships in drug discovery programs.

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