3-Bromo-4-methyl-1H-pyrrolo[3,2-c]pyridine

95%

Reagent Code: #140983
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CAS Number 1000342-72-2

science Other reagents with same CAS 1000342-72-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.06 g/mol
Formula C₈H₇BrN₂
badge Registry Numbers
MDL Number MFCD09749964
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

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 structure enables selective binding to enzyme active sites, making it valuable in drug discovery. Commonly employed in cross-coupling reactions to build complex heterocyclic systems found in bioactive molecules. Also utilized in research for designing novel antiviral and anti-inflammatory agents due to its favorable reactivity and stability in various reaction conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,410.00
inventory 1g
10-20 days ฿47,730.00

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3-Bromo-4-methyl-1H-pyrrolo[3,2-c]pyridine
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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 structure enables selective binding to enzyme active sites, making it valuable in drug discovery. Commonly employed in cross-coupling reactions to build complex heterocyclic systems found in bioactive molecules. Also utilized in research for designing novel antiviral and anti-inflammatory agents due to its favorable reactivity and stability in various rea

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure enables selective binding to enzyme active sites, making it valuable in drug discovery. Commonly employed in cross-coupling reactions to build complex heterocyclic systems found in bioactive molecules. Also utilized in research for designing novel antiviral and anti-inflammatory agents due to its favorable reactivity and stability in various reaction conditions.

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