1313899-55-6

Basic information

• Product Name: C₁₉H₁₅Cl₂NO
• CAS NO: 1313899-55-6
• Molecular Weight: 344.24
• Mol File: 1313899-55-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₉H₁₅Cl₂NO(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₉H₁₅Cl₂NO(1313899-55-6)
• EPA Substance Registry System: C₁₉H₁₅Cl₂NO(1313899-55-6)

Safety Data

• Hazardous Substances Data: 1313899-55-6(Hazardous Substances Data)

Upstream product

• 88-74-4 2-nitro-aniline 
• 827-23-6 2,4-dibromo-6-nitroaniline 
• 116529-58-9 2,3,5-tribromonitrobenzene 
• 1313898-56-4 C₁₃H₁₂BrNO 
• 151169-74-3 2,3-dichlorobenzeneboronic acid 
• 1202382-70-4 C₁₃H₁₀BrNO 
• 1202382-69-1 4,6,7-tribromo-1-methyl-1H-indole 
• 1202382-67-9 4,6,7-tribromo-1H-indole 

Relevant articles and documents

Application of 6,7-indole aryne cycloaddition and Pd(0)-catalyzed Suzuki-Miyaura and Buchwald-Hartwig cross-coupling reactions for the preparation of annulated indole libraries

The construction of an unprecedented class of an indole-based library, namely, a 6,7-annulated-4-substituted 93-member indole library, using a strategic combination of 6,7-indolyne cycloaddition and cross-coupling reactions under both Suzuki-Miyaura and Buchwald-Hartwig conditions is described. This work represents the first example of library development that employs the indole aryne methodology. Annulated indoles, with the exception of only a few biologically active natural products (i.e., the trikentrins, herbindoles, teleocidins, and nodulisporic acids), have no representation in the PubChem or MLSMR databases. These structural entities are therefore predicted to have unique chemical property space characteristics and a high probability of exhibiting interesting biological activity.