2-methoxy-3-nitropyridin-4-amine

≥95%

Reagent Code: #205778
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CAS Number 33623-16-4

science Other reagents with same CAS 33623-16-4

blur_circular Chemical Specifications

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Weight 169.14 g/mol
Formula C₆H₇N₃O₃
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MDL Number MFCD07437848
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

2-Methoxy-3-nitropyridin-4-amine is used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure, featuring a pyridine ring substituted with a methoxy group at position 2, a nitro group at position 3, and an amino group at position 4, allows for further functionalization through reactions such as nitro group reduction to an amine or nucleophilic substitutions at activated positions. This versatility makes it valuable in medicinal chemistry for creating analogs with potential anti-inflammatory, anticancer, or antimicrobial activity. It is also employed in research settings to build complex heterocyclic systems for drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,390.00
inventory 1g
10-20 days ฿9,450.00
inventory 5g
10-20 days ฿34,120.00
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2-methoxy-3-nitropyridin-4-amine
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2-Methoxy-3-nitropyridin-4-amine is used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure, featuring a pyridine ring substituted with a methoxy group at position 2, a nitro group at position 3, and an amino group at position 4, allows for further functionalization through reactions such as nitro group reduction to an amine or nucleophilic substitutions at activated positions. This versatility

2-Methoxy-3-nitropyridin-4-amine is used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure, featuring a pyridine ring substituted with a methoxy group at position 2, a nitro group at position 3, and an amino group at position 4, allows for further functionalization through reactions such as nitro group reduction to an amine or nucleophilic substitutions at activated positions. This versatility makes it valuable in medicinal chemistry for creating analogs with potential anti-inflammatory, anticancer, or antimicrobial activity. It is also employed in research settings to build complex heterocyclic systems for drug discovery.

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