680208-62-2

Basic information

• Product Name: 1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid, 6-Methoxy-
• Synonyms: 1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid, 6-Methoxy-;6-methoxy-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid
• CAS NO: 680208-62-2
• Molecular Formula: C₉H₈N₂O₃
• Molecular Weight: 192.17142
• Mol File: 680208-62-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid, 6-Methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid, 6-Methoxy-(680208-62-2)
• EPA Substance Registry System: 1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid, 6-Methoxy-(680208-62-2)

Safety Data

• Hazardous Substances Data: 680208-62-2(Hazardous Substances Data)

Usage

Derivative of pyrrolopyridine

yes

Used in medicinal chemistry

yes

Potential therapeutic applications

yes

Contains a carboxylic acid group

yes

Contains a methoxy group

yes

Implications for solubility and reactivity

yes

Promising candidate for further research and development in the pharmaceutical industry

yes

Upstream product

• 149539-81-1 methyl 6-amino-2-methoxypyridine-3-carboxylate 
• 65515-32-4 methyl 6-chloro-2-methoxypyridine-3-carboxylate 
• 65515-28-8 methyl 2,6-dichloronicotinate 
• 680208-60-0 6-acetylamino-2-methoxy-5-trimethylsilanylethynyl-nicotinic acid methyl ester 
• 680208-58-6 6-amino-2-methoxy-5-trimethylsilanylethynyl-nicotinic acid methyl ester 
• 680208-55-3 2-methoxy-6-(4-methoxy-benzylamino)-nicotinic acid methyl ester 
• 557106-97-5 methyl 6-amino-5-iodo-2-(methyloxy)-3-pyridinecarboxylate 
• 38496-18-3 2,6-dichloropyridine-3-carboxylic acid 
• 680208-61-1 6-methoxy-1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid methyl ester 

Downstream Products

• 680208-04-2 [4-(4-fluoro-benzyl)-piperidin-1-yl]-(6-methoxy-1H-pyrrolo[2,3-b]pyridin-5-yl)-methanone 

Relevant articles and documents

AZAINDOLE DERIVATIVES AS INHIBITORS OF P38 KINASE

The invention is directed to methods to inhibit p38 kinase, preferably p38-α using compounds which are azaindoles wherein the azaindoles are coupled through an azacyclic linker to another cyclic moiety.