109535-73-1

Basic information

• Product Name: 2H-Pyrrolo[2,3-b]pyridin-2-one, 1,3-dihydro-3,3-diMethyl-
• Synonyms: 2H-Pyrrolo[2,3-b]pyridin-2-one, 1,3-dihydro-3,3-diMethyl-;3,3-Dimethyl-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one;3,3-DiMethyl-1H-pyrrolo[2,3-b]pyridin-2(3H)-one
• CAS NO: 109535-73-1
• Molecular Formula: C₉H₁₀N₂O
• Molecular Weight: 162.1885
• Mol File: 109535-73-1.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 329.712 °C at 760 mmHg
• Flash Point: 153.204 °C
• Appearance: /
• Density: 1.137 g/cm³
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2H-Pyrrolo[2,3-b]pyridin-2-one, 1,3-dihydro-3,3-diMethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyrrolo[2,3-b]pyridin-2-one, 1,3-dihydro-3,3-diMethyl-(109535-73-1)
• EPA Substance Registry System: 2H-Pyrrolo[2,3-b]pyridin-2-one, 1,3-dihydro-3,3-diMethyl-(109535-73-1)

Safety Data

• Hazardous Substances Data: 109535-73-1(Hazardous Substances Data)

Usage

General Description

2H-Pyrrolo[2,3-b]pyridin-2-one, 1,3-dihydro-3,3-dimethyl- is a chemical compound with a molecular formula of C9H11NO. It is a heterocyclic compound that contains a pyrrolopyridine ring structure. The compound is 1,3-dihydro and contains two methyl groups on the third carbon, giving it a 3,3-dimethyl substitution pattern. 2H-Pyrrolo[2,3-b]pyridin-2-one, 1,3-dihydro-3,3-dimethyl- has potential applications in the pharmaceutical industry, particularly in the development of new drugs and therapeutic treatments. Its unique structure and properties make it an interesting target for further research and development.

Upstream product

• 5654-97-7 7-azaoxindole 
• 74-88-4 methyl iodide 
• 1393491-78-5 2-(2-bromopyridin-3-yl)-2-methylpropanenitrile 

Downstream Products

• 1595279-67-6 3,3-dimethyl-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine 
• 1319742-70-5 trans-5-chloro-N-[4-(3,3-dimethyl-2-oxo-2,3-dihydro-pyrrolo[2,3-b]pyridin-1-ylmethyl)-cyclohexyl]-2-methyl-nicotinamide 
• 1319742-69-2 trans-2-chloro-N-[4-(3,3-dimethyl-2-oxo-2,3-dihydro-pyrrolo[2,3-b]pyridin-1-ylmethyl)-cyclohexyl]-5-trifluoromethyl-benzamide 

Relevant articles and documents

HETEROCYCLIC COMPOUNDS AS INHIBITORS OF FATTY ACID BIOSYSNTHESIS FOR BACTERIAL INFECTIONS

The present invention relates to novel heterocyclic compounds which specifically inhibit bacterial FabI and can be used for the treatment of Staphylococcal infections.

Copper-catalyzed domino coupling reaction: An efficient method to synthesize oxindoles

An efficient and novel procedure for a copper catalyzed domino coupling reaction has been developed, which afforded various oxindoles in good to excellent yields with tolerance of various substituents. In addition, this method could be applied to synthesize horsfiline and coerulescine in few steps with high total yields. The Royal Society of Chemistry 2012.

Heterobicyclic compounds having antiinflammatory activity

Heterobicyclic and heterocyclic intermediate compounds and their use in treating inflammation, hyperproliferative skin conditions such as psoriasis and allergy are disclosed.