3-(1-Methyl-1H-pyrrol-2-yl)pyridine

99%

Reagent Code: #203614
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CAS Number 487-19-4

science Other reagents with same CAS 487-19-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.2 g/mol
Formula C₁₀H₁₀N₂
badge Registry Numbers
MDL Number MFCD00468104
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It also serves as a building block in agrochemicals, contributing to the creation of novel pesticides with improved selectivity. Its structure supports coordination in catalytic systems, making it useful in certain metal-catalyzed reactions. Additionally, it is employed in research for designing bioactive molecules due to its ability to mimic natural heterocyclic compounds.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿19,250.00
inventory 25mg
10-20 days ฿51,250.00
inventory 100mg
10-20 days ฿116,080.00

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3-(1-Methyl-1H-pyrrol-2-yl)pyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It also serves as a building block in agrochemicals, contributing to the creation of novel pesticides with improved selectivity. Its structure supports coordination in catalytic systems, making it useful in certain metal-catalyzed reactions. Additionally, it is employed in research for designing bioactive molecules due to its ability to mimic natural heterocyclic comp

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It also serves as a building block in agrochemicals, contributing to the creation of novel pesticides with improved selectivity. Its structure supports coordination in catalytic systems, making it useful in certain metal-catalyzed reactions. Additionally, it is employed in research for designing bioactive molecules due to its ability to mimic natural heterocyclic compounds.

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