111861-26-8

Basic information

• Product Name: 4H-1-Benzopyran-3-carbonitrile, 2-amino-4-(2-fluorophenyl)-7-hydroxy-
• CAS NO: 111861-26-8
• Molecular Formula: C16H11FN2O2
• Molecular Weight: 282.274
• Mol File: 111861-26-8.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 4H-1-Benzopyran-3-carbonitrile, 2-amino-4-(2-fluorophenyl)-7-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1-Benzopyran-3-carbonitrile, 2-amino-4-(2-fluorophenyl)-7-hydroxy-(111861-26-8)
• EPA Substance Registry System: 4H-1-Benzopyran-3-carbonitrile, 2-amino-4-(2-fluorophenyl)-7-hydroxy-(111861-26-8)

Safety Data

• Hazardous Substances Data: 111861-26-8(Hazardous Substances Data)

Upstream product

• 2698-43-3 2-(2-fluorobenzylidene)malononitrile 
• 108-46-3 recorcinol 
• 446-52-6 2-Fluorobenzaldehyde 
• 109-77-3 malononitrile 

Relevant articles and documents

Three-component coupling approach for the synthesis of 4H-pyrans and pyran-annulated heterocyclic scaffolds utilizing Ag/TiO2 nano-thin films as robust recoverable catalyst

As a segment of ongoing surveys and with the aim of expansion of environmentally benign processes, a series of biologically varied type of substituted 2-amino-3-cyano-4H-pyrans and pyran-annulated Scaffolds have been synthesized by tandem Knoevenagel-cycl

Green protocol for synthesis of MgFe2O4 nanoparticles and study of their activity as an efficient catalyst for the synthesis of chromene and pyran derivatives under ultrasound irradiation

In this study, the MgFe2O4 nanoparticles were synthesized via a green and simple approach. Then an effective procedure to synthesize 2-amino-7-hydroxy-4H-chromene and tetrahydrobenzo[b]pyran derivatives was established through the ch

Saccharose as a new, natural, and highly efficient catalyst for the one-pot synthesis of 4,5-dihydropyrano[3,2-c]chromenes, 2-amino-3-cyano-4H-chromenes, 1,8-dioxodecahydroacridine, and 2-substituted benzimidazole derivatives

Saccharose was applied as a green and natural catalyst for the one-pot, three-component condensation between aromatic aldehydes, malononitrile, and resorcinol, or 4-hydroxycoumarine to afford the corresponding pyran-annulated heterocyclic systems. This gr