138469-76-8

Basic information

• Product Name: 1H-Pyrrolo[3,2-b]pyridine, 5-Methoxy-3-Methyl-
• Synonyms: 1H-Pyrrolo[3,2-b]pyridine, 5-Methoxy-3-Methyl-;5-Methoxy-3-Methyl-4-azaindole
• CAS NO: 138469-76-8
• Molecular Formula: C9H10N2O
• Molecular Weight: 162.1885
• EINECS: -0
• Mol File: 138469-76-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 88℃
• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 1H-Pyrrolo[3,2-b]pyridine, 5-Methoxy-3-Methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrolo[3,2-b]pyridine, 5-Methoxy-3-Methyl-(138469-76-8)
• EPA Substance Registry System: 1H-Pyrrolo[3,2-b]pyridine, 5-Methoxy-3-Methyl-(138469-76-8)

Safety Data

• Hazardous Substances Data: 138469-76-8(Hazardous Substances Data)

Usage

General Description

1H-Pyrrolo[3,2-b]pyridine, 5-methoxy-3-methyl- is a chemical compound with the molecular formula C11H11NO. It is a heterocyclic compound consisting of a pyrrolopyridine core with a methoxy and methyl substituent. 1H-Pyrrolo[3,2-b]pyridine, 5-methoxy-3-methyl- is commonly used in organic synthesis and medicinal chemistry as a building block for the preparation of various pharmaceuticals and bioactive molecules. It has shown potential as a drug candidate for the treatment of various diseases and conditions, and studies have been conducted to explore its pharmacological properties and potential therapeutic applications.

Upstream product

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Relevant articles and documents

Active and Recyclable Catalytic Synthesis of Indoles by Reductive Cyclization of 2-(2-Nitroaryl)acetonitriles in the Presence of Co-Rh Heterobimetallic Nanoparticles with Atmospheric Hydrogen under Mild Conditions

A cobalt-rhodium heterobimetallic nanoparticle-catalyzed reductive cyclization of 2-(2-nitroaryl)acetonitriles to indoles has been achieved. The tandem reaction proceeds without any additives under the mild conditions (1 atm H2 and 25 °C). This procedure could be scaled up to the gram scale. The catalytic system is significantly stable under these reaction conditions and could be reused more than ten times without loss of catalytic activity.

Synthesis of C3-substituted 4-azaindoles: An easy access to 4-azamelatonin and protected 4-azatryptophan

(Chemical Equation Presented) C3-Substituted-4-azaindoles were synthesized from pyridylacetonitriles in a two-step sequence allowing the easy introduction of a range of substituents. This strategy permits the rapid synthesis of 4-azamelatonin and a protec

THE USE OF o-NITROARYLACETONITRILES AS CARBON ACID PARTICIPANTS IN THE MITSUNOBU REACTION

The use of o-nitroarylacetonitriles as carbon acids in the Mitsunobu reaction is discussed as a method of carbon-carbon bond formation.This reaction represents a rare example of a carbon acid participating in a Mitsunobu reaction.