6-Bromo-3-methoxypicolinonitrile

95%

Reagent Code: #141339
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CAS Number 393813-61-1

science Other reagents with same CAS 393813-61-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.03 g/mol
Formula C₇H₅BrN₂O
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MDL Number MFCD28128344
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its 6-bromo-3-methoxy substituted pyridine structure with a nitrile group allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in agrochemical research to create novel pesticides with improved efficacy and environmental profiles. Also utilized in materials science for designing organic semiconductors due to its electron-withdrawing nitrile group and halogen functionality.

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inventory 100mg
10-20 days ฿5,170.00

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6-Bromo-3-methoxypicolinonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its 6-bromo-3-methoxy substituted pyridine structure with a nitrile group allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in agrochemical research to create novel pesticides with improved efficacy and environmental profiles. Also utilized in materials science for designing organic semiconduct

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its 6-bromo-3-methoxy substituted pyridine structure with a nitrile group allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in agrochemical research to create novel pesticides with improved efficacy and environmental profiles. Also utilized in materials science for designing organic semiconductors due to its electron-withdrawing nitrile group and halogen functionality.

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