5-Bromo-3-iodo-4,7-diazaindole

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Reagent Code: #145353
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CAS Number 875781-44-5

science Other reagents with same CAS 875781-44-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.92 g/mol
Formula C₆H₃BrIN₃
badge Registry Numbers
MDL Number MFCD09878696
thermostat Physical Properties
Boiling Point 311°C
inventory_2 Storage & Handling
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. Its halogenated structure allows for selective cross-coupling reactions, enabling the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to its ability to modulate electronic and steric properties in drug candidates. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿137.50
inventory 100mg
10-20 days ฿176.00
inventory 500mg
10-20 days ฿693.00
inventory 1g
10-20 days ฿1,690.00
inventory 5g
10-20 days ฿6,200.00

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5-Bromo-3-iodo-4,7-diazaindole
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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. Its halogenated structure allows for selective cross-coupling reactions, enabling the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to its ability to modulate electronic and steric properties in drug candidates. Also utilized in

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its halogenated structure allows for selective cross-coupling reactions, enabling the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to its ability to modulate electronic and steric properties in drug candidates. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays.

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