1444003-20-6

Basic information

• Product Name: (S)-N-(2-acetylphenyl)-3-(3,4-dimethoxyphenyl)-2-(1H-pyrrol-1-yl)propanamide
• Synonyms: (S)-N-(2-acetylphenyl)-3-(3,4-dimethoxyphenyl)-2-(1H-pyrrol-1-yl)propanamide
• CAS NO: 1444003-20-6
• Molecular Weight: 392.455
• Mol File: 1444003-20-6.mol

Chemical Properties

• CAS DataBase Reference: (S)-N-(2-acetylphenyl)-3-(3,4-dimethoxyphenyl)-2-(1H-pyrrol-1-yl)propanamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-N-(2-acetylphenyl)-3-(3,4-dimethoxyphenyl)-2-(1H-pyrrol-1-yl)propanamide(1444003-20-6)
• EPA Substance Registry System: (S)-N-(2-acetylphenyl)-3-(3,4-dimethoxyphenyl)-2-(1H-pyrrol-1-yl)propanamide(1444003-20-6)

Safety Data

• Hazardous Substances Data: 1444003-20-6(Hazardous Substances Data)

Upstream product

• 1444003-11-5 (S)-3-(3,4-dimethoxyphenyl)-2-(1H-pyrrol-1-yl)propanoic acid 
• 551-93-9 2-aminoacetophenone 

Downstream Products

• 1444003-32-0 C₂₆H₃₃N₃O₅ 

Relevant articles and documents

Photoassisted synthesis of enantiopure alkaloid mimics possessing unprecedented polyheterocyclic cores

Enantiopure alkaloid mimics are synthesized via high yielding intramolecular cycloadditions of photogenerated azaxylylenes tethered to pyrroles, with further growth of molecular complexity via post-photochemical transformations of primary photoproducts. This expeditious access to structurally unprecedented polyheterocyclic cores is being developed in the context of diversity-oriented synthesis, as the modular design allows for rapid "pre-assembly" of diverse photoprecursors from simple building blocks/diversity inputs.