3,5-dibromo-N-methylpyridin-2-amine

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Reagent Code: #215214
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CAS Number 858839-25-5

science Other reagents with same CAS 858839-25-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.9332 g/mol
Formula C₆H₆Br₂N₂
thermostat Physical Properties
Melting Point 47-49 °C
Boiling Point 280.3±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.977±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key 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 form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of selective protein kinase C (PKC) modulators and other signaling pathway inhibitors. Its bromine substituents allow for further functionalization via cross-coupling reactions, making it valuable in structure-activity relationship (SAR) studies during drug discovery. Also utilized in agrochemical research for designing novel bioactive molecules with pesticidal or fungicidal properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,800.00
inventory 1g
10-20 days ฿32,000.00

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3,5-dibromo-N-methylpyridin-2-amine
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Used as a key 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 form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of selective protein kinase C (PKC) modulators and other signaling pathway inhibitors. Its bromine substituents allow for further functionalization via cross-coupling reactio

Used as a key 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 form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of selective protein kinase C (PKC) modulators and other signaling pathway inhibitors. Its bromine substituents allow for further functionalization via cross-coupling reactions, making it valuable in structure-activity relationship (SAR) studies during drug discovery. Also utilized in agrochemical research for designing novel bioactive molecules with pesticidal or fungicidal properties.

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