16299-27-7

Basic information

• Product Name: 2H-1-Benzopyran-2-one, 7-(acetyloxy)-4-phenyl-
• CAS NO: 16299-27-7
• Molecular Formula: C17H12O4
• Molecular Weight: 280.28
• Mol File: 16299-27-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2H-1-Benzopyran-2-one, 7-(acetyloxy)-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-1-Benzopyran-2-one, 7-(acetyloxy)-4-phenyl-(16299-27-7)
• EPA Substance Registry System: 2H-1-Benzopyran-2-one, 7-(acetyloxy)-4-phenyl-(16299-27-7)

Safety Data

• Hazardous Substances Data: 16299-27-7(Hazardous Substances Data)

Upstream product

• 131-56-6 2.4-dihydroxybenzophenone 
• 108-24-7 acetic anhydride 
• 2555-30-8 7-hydroxy-4-phenylcoumarin 
• 75-36-5 acetyl chloride 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 108-46-3 recorcinol 

Downstream Products

• 59257-85-1 2,2-dimethyl-4-phenyl-2H-chromen-7-ol 
• 2555-30-8 7-hydroxy-4-phenylcoumarin 
• 54431-18-4 8-acetyl-7-hydroxy-4-phenyl-2H-1-benzopyran-2-one 
• 94739-98-7 6-Acetyl-7-hydroxy-4-phenyl-chromen-2-one 
• 945750-60-7 C₁₉H₁₀O₅ 
• 66262-41-7 8-benzoyl-7-methoxy-4-phenyl-chromen-2-one 
• 94739-93-2 2-oxo-4-phenyl-2H-chromen-7-ylbenzoate 
• 94739-99-8 6-benzoyl-7-hydroxy-4-phenyl-coumarin 
• 90104-86-2 8-benzoyl-7-hydroxy-4-phenyl-coumarin 
• 57391-60-3 8-acetyl-7-methoxy-4-phenyl-chromen-2-one 
• 94739-96-5 7-furoyloxy-4-phenylcoumarin 
• 94739-94-3 7-hexanoyloxy-4-phenylcoumarin 
• 94739-95-4 7-(β,β-dimethylacryloxy)-4-phenylcoumarin 
• 482-82-6 nordalbergin 

Relevant articles and documents

Synthesis, computational studies and assessment of in vitro inhibitory activity of umbelliferon-based compounds against tumour-associated carbonic anhydrase isoforms IX and XII

Coumarins are widely diffused secondary metabolites possessing a plethora of biological activities. It has been established that coumarins represent a peculiar class of human carbonic anhydrase (hCA) inhibitors having a distinct mechanism of action involv

Synthesis and biological activity of meso-tetrakis (2,10-dioxo-2H, 10H-pyrano [2,3-f] chromene-9-yl) porphyrins

Synthesis of meso-tetrakis (2, 10-dioxo-2H, 10H-pyrano[2,3-f] chromene-9-yl) porphyrins are synthesized directly by reaction of pyrrole with substituted 4-methyl-2,10-dioxo-2H, 10H-pyrano[2,3-f]chromene-9-carbaldehydes in dichloromethane / acid media. The aldehyde's molar ratio was controlled to optimize the synthesis and purification of the desired porphyrins. This new series of porphyrins was characterized by TLC, Mass Spectrometry (FAB mass), 1H NMR, UV and IR ARKAT.