Methyl 5-amino-6-methoxynicotinate

≥95%

Reagent Code: #208797
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CAS Number 59237-50-2

science Other reagents with same CAS 59237-50-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.18 g/mol
Formula C₈H₁₀N₂O₃
badge Registry Numbers
MDL Number MFCD20697606
thermostat Physical Properties
Boiling Point 334.8±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of heterocyclic systems common in drug design. Commonly employed in research settings for medicinal chemistry projects, especially in the optimization of lead compounds for improved potency and selectivity. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,280.00
inventory 250mg
10-20 days ฿2,470.00
inventory 1g
10-20 days ฿8,120.00
inventory 5g
10-20 days ฿35,510.00

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Methyl 5-amino-6-methoxynicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of heterocyclic systems common in drug design. Commonly employed in research settings for medicinal chemistry projects, especially in the optimization of lead compounds for improved potency and selectivity. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of heterocyclic systems common in drug design. Commonly employed in research settings for medicinal chemistry projects, especially in the optimization of lead compounds for improved potency and selectivity. Also utilized in the preparation of analogs for structure-activity relationship (SAR) studies.

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