2-Methoxy-6-Methylpyridin-4-Amine

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Reagent Code: #207827
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CAS Number 89943-09-9

science Other reagents with same CAS 89943-09-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.16 g/mol
Formula C₇H₁₀N₂O
badge Registry Numbers
MDL Number MFCD15529703
thermostat Physical Properties
Boiling Point 275.2°C at 760 mmHg
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 agrochemicals for creating herbicides and fungicides due to its stable heterocyclic structure. Also employed in research for designing new bioactive molecules with antimicrobial or anti-inflammatory properties. Its amine and methoxy groups allow for easy functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,940.00
inventory 1g
10-20 days ฿4,900.00
inventory 5g
10-20 days ฿24,360.00

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2-Methoxy-6-Methylpyridin-4-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 agrochemicals for creating herbicides and fungicides due to its stable heterocyclic structure. Also employed in research for designing new bioactive molecules with antimicrobial or anti-inflammatory properties. Its amine and methoxy groups allow for easy functionalization, making it valuable in medicinal chemistry for structure-activity r

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 agrochemicals for creating herbicides and fungicides due to its stable heterocyclic structure. Also employed in research for designing new bioactive molecules with antimicrobial or anti-inflammatory properties. Its amine and methoxy groups allow for easy functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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