71058-41-8

Basic information

• Product Name: 1H-Pyrrolo[3,4-c]pyridine-1,3(2H)-dione, 7-amino-6-methyl-2-phenyl-
• CAS NO: 71058-41-8
• Molecular Formula: C14H11N3O2
• Molecular Weight: 253.26
• Mol File: 71058-41-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrolo[3,4-c]pyridine-1,3(2H)-dione, 7-amino-6-methyl-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrolo[3,4-c]pyridine-1,3(2H)-dione, 7-amino-6-methyl-2-phenyl-(71058-41-8)
• EPA Substance Registry System: 1H-Pyrrolo[3,4-c]pyridine-1,3(2H)-dione, 7-amino-6-methyl-2-phenyl-(71058-41-8)

Safety Data

• Hazardous Substances Data: 71058-41-8(Hazardous Substances Data)

Usage

Explanation

This is the formal name of the chemical compound, which describes its structure and the functional groups present.
2. Complex Structure

Explanation

The compound has a intricate arrangement of atoms and bonds, featuring a pyrrolopyridine core with various substituents.
3. Pyrrolopyridine Core

Explanation

The central framework of the compound consists of a fusion of a pyrrole and a pyridine ring, which are both heterocyclic aromatic rings.
4. Amino Group (-NH2)

Explanation

An amino group is a functional group consisting of a nitrogen atom bonded to two hydrogen atoms. It is attached to the 7-position of the pyrrolopyridine core.
5. Methyl Group (-CH3)

Explanation

A methyl group is an alkyl group with one carbon atom and three hydrogen atoms. It is attached to the 6-position of the pyrrolopyridine core.
6. Phenyl Group (C6H5-)

Explanation

A phenyl group is a carbon-based functional group consisting of a six-membered aromatic ring with five carbon atoms and one hydrogen atom. It is attached to the 2-position of the pyrrolopyridine core.
7. Heterocyclic Compound

Explanation

The compound is classified as a heterocyclic compound because it contains at least one ring with non-carbon atoms (such as nitrogen) in the structure.
8. Organic Reactions and Synthesis

Explanation

The compound can participate in various organic reactions due to its unique structure and functional groups, making it a valuable building block in organic synthesis.
9. Potential Applications in Medicinal Chemistry and Drug Development

Explanation

The compound's unique structure and functional groups may provide new opportunities in the design and development of pharmaceuticals and therapeutic agents.
10. Material Science Applications

Explanation

The compound could be used in the development of new materials with specific properties, such as optical, electronic, or mechanical characteristics, due to its heterocyclic nature and functional groups.
11. Further Research Necessary

Explanation

More research is needed to fully explore the potential and applications of this compound in various scientific fields, including its reactivity, stability, and potential uses in different industries.

Upstream product

• 941-69-5 N-phenyl-maleimide 
• 114362-29-7 ((1R,2S,6R,7S)-9-Methyl-3,5-dioxo-4-phenyl-10-oxa-4,8-diaza-tricyclo[5.2.1.0^2,6]dec-8-en-1-yl)-carbamic acid benzyl ester 
• 27394-99-6 N-(α-cyanoethyl)formamide 

Downstream Products

• 90330-14-6 7-amino-6-(2,5-dioxo-1-phenylpyrrolidin-3-yl)methyl-1,3-dioxo-2-phenyl-1,3-dihydropyrrolo<3,4-c>pyridine 

Relevant articles and documents

Reaction of 5-(Substituted-amino)oxazoles with N-Phenylmaleimide

Reaction of 5-aminooxazoles with N-phenylmaleimide gave 7-hydroxy-2-phenylpyrrolopyridine-1,3-diones and 7-amino-2-phenylpyrrolopyridine-1,3-diones via tricyclic adducts.The ratio of the 7-hydroxy compound and 7-amino compound depended on th