6-Methoxy-4-methylpyridin-3-amine

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98%

Reagent Code: #206531
$product.alias - string(0) ""
product.cas - string(9) "6635-91-2"
product.physical_n_chem_properties - string(0) ""
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CAS Number 6635-91-2

science Other reagents with same CAS 6635-91-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.17 g/mol
Formula C₇H₁₀N₂O
thermostat Physical Properties
Melting Point 157-161°C
Boiling Point 280.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, 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 hydrogen bonds and participate in aromatic interactions, enhancing drug binding affinity. Also employed in the preparation of agrochemicals and functional materials where nitrogen-containing heterocycles are required. Its methoxy and amino groups allow for further chemical modifications, making it valuable in structure-activity relationship studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿620.00
inventory 5g
10-20 days ฿2,280.00
inventory 25g
10-20 days ฿9,980.00

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6-Methoxy-4-methylpyridin-3-amine
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Used as an intermediate in the synthesis of pharmaceuticals, 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 hydrogen bonds and participate in aromatic interactions, enhancing drug binding affinity. Also employed in the preparation of agrochemicals and functional materials where nitrogen-containing heterocycles are required. Its methoxy and amino groups allow for further chemical modifications, making
Used as an intermediate in the synthesis of pharmaceuticals, 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 hydrogen bonds and participate in aromatic interactions, enhancing drug binding affinity. Also employed in the preparation of agrochemicals and functional materials where nitrogen-containing heterocycles are required. Its methoxy and amino groups allow for further chemical modifications, making it valuable in structure-activity relationship studies.
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