454703-31-2

Basic information

• Product Name: 2H-Pyran-3-carbonitrile, 2-oxo-6-phenyl-4-(1-pyrrolidinyl)-
• Synonyms: 2-oxo-6-phenyl-4-pyrrolidino-2H-pyran-3-carbonitrile;2-oxo-6-phenyl-4-pyrrolidin-1-yl-2H-pyran-3-carbonitrile
• CAS NO: 454703-31-2
• Molecular Formula: C16H14N2O2
• Molecular Weight: 266.299
• Mol File: 454703-31-2.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2H-Pyran-3-carbonitrile, 2-oxo-6-phenyl-4-(1-pyrrolidinyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran-3-carbonitrile, 2-oxo-6-phenyl-4-(1-pyrrolidinyl)-(454703-31-2)
• EPA Substance Registry System: 2H-Pyran-3-carbonitrile, 2-oxo-6-phenyl-4-(1-pyrrolidinyl)-(454703-31-2)

Safety Data

• Hazardous Substances Data: 454703-31-2(Hazardous Substances Data)

Upstream product

• 123-75-1 pyrrolidine 
• 61380-85-6 6-phenyl-3-cyano-4-methylsulfanyl-2H-pyran-2-one 
• 98-86-2 acetophenone 

Downstream Products

• 1537881-57-4 10-phenyl-8-(pyrrolidin-1-yl)fluoranthene-7-carbonitrile 
• 1392299-49-8 7-phenyl-9-(pyrrolidin-1-yl)-5,6-dihydrobenzo[f]quinoline-10-carbonitrile 
• 1122565-47-2 1-phenyl-3-pyrrolidin-1-yl-9H-fluorene-4-carbonitrile 
• 1122565-49-4 4-phenyl-2-pyrrolidin-1-yl-9H-fluorene-1-carbonitrile 

Relevant articles and documents

Transition metal-free synthesis of sterically hindered allylarenes from 5-hexene-2-one

A simple, efficient and transition metal-free strategy was established for the synthesis of highly functionalized, sterically hindered allylarenes (6, 7 & 8) by base-mediated ring transformation of 2-oxo-6-aryl-4-(methylthio/sec-amino)-2H-pyran-3-carbonit

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Non-aggregating solvatochromic bipolar benzo[f]quinolines and benzo[a]acridines for organic electronics

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