1577232-57-5

Basic information

• Product Name: C₂₈H₂₂O₃
• Synonyms: C₂₈H₂₂O₃
• CAS NO: 1577232-57-5
• Molecular Weight: 406.481
• Mol File: 1577232-57-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₂₈H₂₂O₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₈H₂₂O₃(1577232-57-5)
• EPA Substance Registry System: C₂₈H₂₂O₃(1577232-57-5)

Safety Data

• Hazardous Substances Data: 1577232-57-5(Hazardous Substances Data)

Upstream product

• 827348-43-6 2-(benzylamino)-5,5-dimethyl-1,3,2-dioxaphosphinane 2-oxide 
• 932-87-6 1-Bromo-2-phenylacetylene 
• 38352-75-9 ethyl 2-acetyl-2-(prop-2-ynyl)pent-4-ynoate 

Downstream Products

• 1577232-40-6 ethyl 2-acetyl-7-bromo-5-phenyl-4-(phenylethynyl)-2,3-dihydro-1H-indene-2-carboxylate 
• 1577232-41-7 ethyl 2-acetyl-7-chloro-5-phenyl-4-(phenylethynyl)-2,3-dihydro-1H-indene-2-carboxylate 
• 1577232-42-8 ethyl 2-acetyl-7-iodo-5-phenyl-4-(phenylethynyl)-2,3-dihydro-1H-indene-2-carboxylate 

Relevant articles and documents

Palladium-catalyzed imidoylative cyclization of α-isocyanoacetamides: Efficient access to c2-diversified oxazoles

A novel procedure for the synthesis of C2-diversified oxazoles, through palladium-catalyzed imidoylative cyclization of α-isocyanoacetamides with aryl, vinyl, alkynyl halides, or triflates, was developed. Migratory insertion of isocyanide into a C sp 3-palladium(II) intermediate in a cascade process was also realized, generating alkyl-substituted oxazoles. Therefore, oxazoles functionalized at the C2 position with sp, sp2, and sp3 hybridized carbon atoms are accessible by applying this method.