Ethyl 2-amino-6-methylnicotinate

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Reagent Code: #184513
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CAS Number 70959-85-2

science Other reagents with same CAS 70959-85-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.20 g/mol
Formula C₉H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD16610933
thermostat Physical Properties
Melting Point 88 °C
Boiling Point 275.2±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.158±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acid derivatives with potential antihypertensive and anti-inflammatory activities. It serves as a building block in the preparation of pyridine-based compounds for medicinal chemistry research. Also employed in the design of kinase inhibitors and other biologically active molecules due to its ability to participate in cyclization and condensation reactions. Its amino and ester functional groups allow for easy modification, making it valuable in combinatorial chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,450.00
inventory 250mg
10-20 days ฿20,900.00
inventory 1g
10-20 days ฿55,100.00

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Ethyl 2-amino-6-methylnicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acid derivatives with potential antihypertensive and anti-inflammatory activities. It serves as a building block in the preparation of pyridine-based compounds for medicinal chemistry research. Also employed in the design of kinase inhibitors and other biologically active molecules due to its ability to participate in cyclization and condensation reactions. Its amino and ester functional groups al

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acid derivatives with potential antihypertensive and anti-inflammatory activities. It serves as a building block in the preparation of pyridine-based compounds for medicinal chemistry research. Also employed in the design of kinase inhibitors and other biologically active molecules due to its ability to participate in cyclization and condensation reactions. Its amino and ester functional groups allow for easy modification, making it valuable in combinatorial chemistry and drug discovery.

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