412027-80-6

Basic information

• Product Name: 7-hydroxy-5-methoxy-4-oxo-2-phenyl-4H-chromene-6-carbaldehyde
• Synonyms: 7-hydroxy-5-methoxy-4-oxo-2-phenyl-4H-chromene-6-carbaldehyde
• CAS NO: 412027-80-6
• Molecular Weight: 296.279
• Mol File: 412027-80-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 7-hydroxy-5-methoxy-4-oxo-2-phenyl-4H-chromene-6-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 7-hydroxy-5-methoxy-4-oxo-2-phenyl-4H-chromene-6-carbaldehyde(412027-80-6)
• EPA Substance Registry System: 7-hydroxy-5-methoxy-4-oxo-2-phenyl-4H-chromene-6-carbaldehyde(412027-80-6)

Safety Data

• Hazardous Substances Data: 412027-80-6(Hazardous Substances Data)

Upstream product

• 1232-43-5 pinnatin 
• 54437-44-4 1-(6-hydroxy-4-methoxybenzo[b]furan-5-yl)-3-phenylprop-2-en-1-one 
• 82-57-5 visnagin 
• 100-52-7 benzaldehyde 
• 484-27-5 5-acetyl-4-methoxybenzofuran-6-ol 
• 7664-93-9 sulfuric acid 
• 64-19-7 acetic acid 

Downstream Products

• 1260141-45-4 N-ethyl-2-((7-hydroxy-5-methoxy-4-oxo-2-phenyl-4H-chromen-6-yl)methylene)hydrazinecarbothioamide 
• 1260141-46-5 N-allyl-2-((7-hydroxy-5-methoxy-4-oxo-2-phenyl-4H-chromen-6-yl)methylene)hydrazinecarbothioamide 
• 1260141-35-2 2-((7-hydroxy-5-methoxy-4-oxo-2-phenyl-4H-chromen-6-yl)methylene)hydrazinecarbothioamide 
• 1260141-44-3 2-((7-hydroxy-5-methoxy-4-oxo-2-phenyl-4H-chromen-6-yl)methylene)-N-methylhydrazinecarbothioamide 
• 1260141-47-6 2-((7-hydroxy-5-methoxy-4-oxo-2-phenyl-4H-chromen-6-yl)methylene)-N-phenylhydrazinecarbothioamide 
• 1616883-52-3 8-allyl-7-hydroxy-5-methoxy-4-oxo-2-phenyl-4H-chromene-6-carbaldehyde 
• 1616883-51-2 C₂₀H₁₆O₅ 
• 491-67-8 5,6,7-trihydroxy-2-phenyl-4H-1-benzopyran-4-one 
• 150036-33-2 6,7-dihydroxy-5-methoxyflavone 

Relevant articles and documents

Design, synthesis and structure-activity relationship of novel semi-synthetic flavonoids as antiproliferative agents

Various flavonoid scaffold based derivatives viz furochalcones (3a-e, 6a-d and 9a-d), furoflavones (10a-d, 11a-d, 12a-d, 18a&b), flavones (21a-d), furoaurones (13a,b, 14a-d and 15a-d) and 7-styrylfurochromones (22a-d and 25a-e) were designed and synthesiz