54916-66-4

Usage

Uses

Used in Pharmaceutical Industry:
5-Bromo-2-methoxy-nicotinic acid is used as an intermediate in the synthesis of pharmaceutical compounds for its unique properties and potential medicinal applications. Its bioactivity and ability to be incorporated into new drug molecules make it a promising candidate for the development of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Bromo-2-methoxy-nicotinic acid is used as a building block for the synthesis of new agrochemical compounds, leveraging its unique properties to create innovative products with potential applications in agriculture and pest control.
Used in Chemical Research:
5-Bromo-2-methoxy-nicotinic acid is used as a ligand for metal complexes and catalysts in chemical research, contributing to the development of new catalysts and materials with improved performance and selectivity.
Used in Organic Synthesis:
As a derivative of nicotinic acid, 5-Bromo-2-methoxy-nicotinic acid is used as an intermediate in organic synthesis, enabling the creation of a wide range of chemical compounds with diverse applications across various industries.

InChI:InChI=1/C7H6BrNO3/c1-12-6-5(7(10)11)2-4(8)3-9-6/h2-3H,1H3,(H,10,11)

Upstream product

• 16498-81-0 2-methoxynicotinic acid 

Downstream Products

• 213193-29-4 5-Bromo-2-methoxy-nicotinic acid ethyl ester 
• 1245646-66-5 5-bromo-2-methoxynicotinamide 
• 893440-50-1 2-(methyloxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinamine 
• 1429297-51-7 C₁₅H₁₅NO₄ 
• 1429297-56-2 C₂₅H₂₄Cl₂FN₅O₂ 
• 1429297-55-1 C₂₆H₂₆Cl₂FN₅O₂ 
• 1429297-54-0 C₂₂H₁₆Cl₂FN₃O₄ 
• 1429297-53-9 C₁₅H₁₂Cl₂FNO₃ 
• 1429297-52-8 C₁₅H₁₄Cl₂FNO₃ 
• 1429297-23-3 C₂₂H₂₀Cl₂FN₃O₅S 
• 1429297-22-2 C₂₅H₂₄Cl₂FN₃O₄ 
• 1429297-21-1 C₂₀H₂₂Cl₂FN₃O₃ 
• 1429297-20-0 C₁₉H₁₉Cl₂FN₂O₄ 
• 1429297-19-7 C₂₂H₂₂Cl₂FN₅O₃ 

Relevant academic research and scientific papers

Synthetic method of 2-methoxyl-3-amino-5-pyridineboronic acid pinacol ester and intermediate thereof

The invention relates to a synthetic method of 2-methoxyl-3-amino-5-pyridineboronic acid pinacol ester and an intermediate thereof. Specifically, the synthetic method is characterized in that the 2-methoxyl-3-amino-5-pyridineboronic acid pinacol ester is obtained by the steps of taking 2-methoxylnicotinic acid as a starting raw material, halogenating, degrading, deprotecting and coupling. The method disclosed by the invention has the advantages of being short in synthesis route, simple, convenient, low in economic cost and highly suitable for industrial production.

TETRACYCLIC HETEROCYCLE COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES

The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

TETRACYCLIC HETEROCYCLE COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES

The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.