10299-69-1

Basic information

• Product Name: 1H-Pyrrolo[2,3-b]pyridine, 2,3-dimethyl-
• Synonyms: 1H-Pyrrolo[2,3-b]pyridine, 2,3-dimethyl-;2,3-diMethyl-7-aza-1H-indole;2,3-DiMethyl-7-azaindole;2,3-dimethyl-1H-pyrrolo[2,3-b]pyridine
• CAS NO: 10299-69-1
• Molecular Formula: C₉H₁₀N₂
• Molecular Weight: 146.1891
• Mol File: 10299-69-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 136-138 °C
• Boiling Point: 348.6±15.0 °C(Predicted)
• Appearance: /
• Density: 1.145 g/cm³
• Refractive Index: 1.644
• PKA: 8.07±0.40(Predicted)
• CAS DataBase Reference: 1H-Pyrrolo[2,3-b]pyridine, 2,3-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrolo[2,3-b]pyridine, 2,3-dimethyl-(10299-69-1)
• EPA Substance Registry System: 1H-Pyrrolo[2,3-b]pyridine, 2,3-dimethyl-(10299-69-1)

Safety Data

• Hazardous Substances Data: 10299-69-1(Hazardous Substances Data)

Usage

General Description

1H-Pyrrolo[2,3-b]pyridine, 2,3-dimethyl- is a chemical compound with the molecular formula C9H9N3. It exists in a liquid state at standard temperature and pressure. This substance is an extremely weak basic (essentially neutral) compound. While it does not have any specific applications or uses mentioned in available databases, it likely could be used in chemical synthesis and research due to its structural properties - possessing both pyrrole and pyridine rings. As with most chemical substances, appropriate safety measures must be taken during its handling and storage.

InChI:InChI=1/C9H10N2/c1-6-7(2)11-9-8(6)4-3-5-10-9/h3-5H,1-2H3,(H,10,11)

Upstream product

• 42330-59-6 (2-chloropyrid-3-yl)methanol 
• 2942-59-8 2-chloronicotinic acid 
• 149489-03-2 tert-butyl (3-ethylpyridin-2-yl)carbamate 
• 4930-98-7 pyrid-2-ylhydrazine 
• 78-93-3 butanone 
• 49609-84-9 2-Chloronicotinoyl chloride 
• 111108-72-6 (2-chloro-3-pyridinyl)methyl bromide 
• 138343-75-6 tert-butyl (3-methylpyridin-2-yl)carbamate 
• 1603-40-3 3-methylpyridin-2-ylamine 

Downstream Products

• 751452-00-3 2,3Dimethyl-7-(p-cyanophenacyl)pyrrolo[2,3-b]pyridine 
• 145958-93-6 2,3-Dimethyl-7-(p-bromophenacyl)pyrrolo[2,3-b]pyridine, hydrobromide 
• 145934-22-1 2,3-Dimethyl-7-(o-carboxyphenethyl)pyrrolo[2,3-b]pyridine 
• 145933-93-3 2,3-Dimethyl-7(2-trifluoromethylphenacyl)-pyrrolo[2,3-b]pyridine hydrobromide 
• 114570-21-7 1-(2,3-Dimethyl-pyrrolo[2,3-b]pyridin-1-yl)-2-hydroxy-2,2-diphenyl-ethanone 
• 784110-57-2 2,3-Dimethyl-7-(p-fluorophenacyl)pyrrolo[2,3.-b ]pyridine 

Relevant articles and documents

Oxidative cleavage reaction of substituted indoles catalyzed by plant cell cultures

We have developed a novel method for the oxidative cleavage of indole carbon double bonds in the presence of H2O2 using plant cell cultures as peroxidase. The oxidative method has some advantage, as features such as mild reactions, good yields, easy work-up and safety.

A convenient method for the preparation of 5-, 6- and 7-azaindoles and their derivatives

The directed ortho lithiation of 2-tert-butoxycarbonylamino-3-methylpyridine (6a) has provided a convenient method for the preparation of 1H-pyrrolo[2,3-b]pyridine (4a, 7-azaindole). This procedure has been used to prepare a range of 3-substituted 2-tert-butoxycarbonylaminopyridines 6, 2- and 3-substituted and 2,3-disubstituted 1H-pyrrolo[2,3-b]pyridines 4 and shown to be of value in the preparation of 1H-pyrrolo[3,2-c]pyridine (15, 5-azaindole) and 1H-pyrrolo[2,3-c]pyridine (18, 6-azaindole) and derivatives.