Methyl 3-amino-2-methoxyisonicotinate

≥95%

Reagent Code: #208845
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CAS Number 175965-76-1

science Other reagents with same CAS 175965-76-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.18 g/mol
Formula C₈H₁₀N₂O₃
badge Registry Numbers
MDL Number MFCD21288103
thermostat Physical Properties
Boiling Point 301.6±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting cancer and inflammatory diseases. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and selectivity. Its ester and amino functionalities allow for easy modification in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,460.00
inventory 250mg
10-20 days ฿3,580.00

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Methyl 3-amino-2-methoxyisonicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting cancer and inflammatory diseases. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and selectivity. Its ester and amino functionalities allow for easy modification

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting cancer and inflammatory diseases. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and selectivity. Its ester and amino functionalities allow for easy modification in multi-step organic syntheses.

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