56807-26-2

Basic information

• Product Name: 2,4-diphenyl-9H-pyrimido[4,5-b]indole
• Synonyms: 2,4-diphenyl-9H-pyrimido[4,5-b]indole
• CAS NO: 56807-26-2
• Molecular Weight: 321.381
• Mol File: 56807-26-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2,4-diphenyl-9H-pyrimido[4,5-b]indole(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-diphenyl-9H-pyrimido[4,5-b]indole(56807-26-2)
• EPA Substance Registry System: 2,4-diphenyl-9H-pyrimido[4,5-b]indole(56807-26-2)

Safety Data

• Hazardous Substances Data: 56807-26-2(Hazardous Substances Data)

Upstream product

• 36946-70-0 indoleamine 
• 100-52-7 benzaldehyde 
• 98-80-6 phenylboronic acid 
• 167558-54-5 2-(2,2-dibromo-vinyl)-phenylamine 
• 139409-34-0 2-bromo-1H-indole 
• 213599-19-0 1-bromo-2-(2,2-dibromovinyl)benzene 
• 59-48-3 2-oxoindole 
• 100-47-0 benzonitrile 

Relevant articles and documents

Base-promoted aerobic oxidative synthesis of fused 1,3,5-triazines under metal-free conditions

An efficient base-promoted aerobic oxidation reaction for the synthesis of fused 1,3,5-triazines from 2-aminobenzimidazoles, aromatic aldehydes, and ammonium iodide has been developed. In this multi-component protocol, ammonium iodide served as a convenient nitrogen source and four C-N bonds were formed in one pot under metal-free conditions. This journal is

A 9H - pyrimido [4, 5 - b] indole synthetic method of the compound

The invention discloses a synthesis method for 9H-pyrimido(4,5-b) indole compounds, and belongs to the technical field of organic synthesis. The synthesis method is characterized by comprising the following steps: dissolving 1-bromine-2-(2,2-dibromoethyle

A novel and simple synthesis of 9H-pyrimido[4,5-b] indoles under microwave irradiation and solvent-free conditions

A novel synthesis of 9H-pyrimido[4,5-b]indoles is described from a simple microwave-assisted reaction between oxindoles and aryl nitriles under solvent-free conditions in good to excellent yields. Georg Thieme Verlag Stuttgart.