4-(3-Bromopyridin-2-yl)morpholine

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Reagent Code: #149146
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CAS Number 54231-38-8

science Other reagents with same CAS 54231-38-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.10 g/mol
Formula C₉H₁₁BrN₂O
badge Registry Numbers
MDL Number MFCD00498942
thermostat Physical Properties
Melting Point 94-95 °C
Boiling Point 337.1 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.499 g/cm3
Storage 2-8°C, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to participate in cross-coupling reactions, enabling the construction of complex heterocyclic systems. Its structure supports binding interactions with biological targets, making it valuable in drug discovery programs focused on oncology and inflammatory diseases. Also employed in the preparation of pyridine-based derivatives with potential neurological activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,120.00
inventory 5g
10-20 days ฿11,580.00

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4-(3-Bromopyridin-2-yl)morpholine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to participate in cross-coupling reactions, enabling the construction of complex heterocyclic systems. Its structure supports binding interactions with biological targets, making it valuable in drug discovery programs focused on oncology and inflammatory diseases. Also employed in the prepar

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to participate in cross-coupling reactions, enabling the construction of complex heterocyclic systems. Its structure supports binding interactions with biological targets, making it valuable in drug discovery programs focused on oncology and inflammatory diseases. Also employed in the preparation of pyridine-based derivatives with potential neurological activity.

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