1384984-04-6

Basic information

• Product Name: 2-phenyl-2H-chromene-6-carbonitrile
• Synonyms: 2-phenyl-2H-chromene-6-carbonitrile
• CAS NO: 1384984-04-6
• Molecular Weight: 233.269
• Mol File: 1384984-04-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-phenyl-2H-chromene-6-carbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-2H-chromene-6-carbonitrile(1384984-04-6)
• EPA Substance Registry System: 2-phenyl-2H-chromene-6-carbonitrile(1384984-04-6)

Safety Data

• Hazardous Substances Data: 1384984-04-6(Hazardous Substances Data)

Upstream product

• 33143-95-2 2H-1-benzopyran-6-carbonitrile 
• 14371-10-9 (E)-3-phenylpropenal 
• 7148-78-9 3,3-diethoxyl-1-phenylprop-1-ene 
• 767-00-0 4-cyanophenol 

Downstream Products

• 1449311-87-8 6-cyano-2-phenyl-3,4-epoxy-chromene 
• 1449312-11-1 6-cyano-(2R)-phenyl-(3S)-camphor(16S,19R)-sulfonylester chromene 

Relevant articles and documents

Bimolecular coupling reactions through oxidatively generated aromatic cations: Scope and stereocontrol

Chromenes, isochromenes, and benzoxathioles react with 2,3-dichloro-5,6- dicyano-1,4-benzoquinone to form stable aromatic cations that react with a range of nucleophiles. These oxidative fragment coupling reactions provide rapid access to structurally div

Aromatic cations from oxidative carbon-hydrogen bond cleavage in bimolecular carbon-carbon bond forming reactions

Chromenes and isochromenes react quickly with 2,3-dichloro-5,6-dicyano-1,4- benzoquinone (DDQ) to form persistent aromatic oxocarbenium ions through oxidative carbon-hydrogen cleavage. This process is tolerant of electron-donating and electron-withdrawing groups on the benzene ring and additional substitution on the pyran ring. A variety of nucleophiles can be added to these cations to generate a diverse set of structures.