N1-(5-Bromopyrid-2-yl)ethane-1,2-diamine

96%

Reagent Code: #218120
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CAS Number 199522-66-2

science Other reagents with same CAS 199522-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.08 g/mol
Formula C₇H₁₀BrN₃
badge Registry Numbers
MDL Number MFCD07784020
thermostat Physical Properties
Boiling Point 327.529°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

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 form stable heterocyclic structures. Commonly employed in the preparation of pyridine-based drug candidates targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing novel pesticides with improved selectivity. Its bromo and amine functional groups allow for further derivatization via cross-coupling reactions or nucleophilic substitution.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,000.00
inventory 250mg
10-20 days ฿1,790.00
inventory 1g
10-20 days ฿4,810.00
inventory 5g
10-20 days ฿16,830.00

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N1-(5-Bromopyrid-2-yl)ethane-1,2-diamine
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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 form stable heterocyclic structures. Commonly employed in the preparation of pyridine-based drug candidates targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing novel pesticides with improved selectivity. Its bromo and amine func

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 form stable heterocyclic structures. Commonly employed in the preparation of pyridine-based drug candidates targeting inflammatory diseases and neurological disorders. Also utilized in agrochemical research for designing novel pesticides with improved selectivity. Its bromo and amine functional groups allow for further derivatization via cross-coupling reactions or nucleophilic substitution.

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