40649-75-0

Upstream product

• 64-17-5 ethanol 
• 623-11-0 1-methyl-4-nitrosobenzene 
• 874486-85-8 1-(1-acetoxy-[2]naphthyl)-2,3-epoxy-3-(4-methoxy-phenyl)-propan-1-one 
• 711-79-5 1-hydroxy-2-acetonaphthone 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 116491-40-8 6-(4-Methoxy-phenyl)-6H-5-oxa-11,12-diaza-benzo[b]chrysene 
• 30508-15-7 5'-Bromo-2'-hydroxy-4-methoxy-3',4'-benzochalkone α,β-dibromide 
• 98166-67-7 UCCF 355 
• 22876-96-6 2-(5-(4-methoxyphenyl)-4,5-dihydro-1H-pyrazol-3-yl)naphthalen-1-ol 
• 1446419-69-7 3-(1-hydroxynaphthalen-2-yl)-5-bis(4-methoxyphenyl)-N-(3,4,5-trimethoxyphenyl)-2-pyrazoline-1-carbothioamide 
• 1446419-68-6 N-(2,4-dimethoxyphenyl)-3-(1-hydroxynaphthalen-2-yl)-5-(4-methoxyphenyl)-2-pyrazoline-1-carbothioamide 
• 1446419-67-5 3-(1-hydroxynaphthalen-2-yl)-N,5-bis(4-methoxyphenyl)-2-pyrazoline-1-carbothioamide 
• 1446419-66-4 3-(1-hydroxynaphthalen-2-yl)-N-(3-methoxyphenyl)-5-(4-methoxyphenyl)-2-pyrazoline-1-carbothioamide 
• 1446419-65-3 3-(1-hydroxynaphthalen-2-yl)-N-(2-methoxyphenyl)-5-(4-methoxyphenyl)-2-pyrazoline-1-carbothioamide 
• 1446419-64-2 3-(1-hydroxynaphthalen-2-yl)-5-(4-methoxyphenyl)-N-phenyl-2-pyrazoline-1-carbothioamide 
• 14756-22-0 UCCF 269 
• 129457-15-4 nickel(II){3-(1-hydroxy-2-naphthyl)-5-(4-MeO-phenyl)pyrazoline}2 
• 129457-18-7 nickel(II){3-(1-hydroxy-2-naphthyl)-5-(4-MeO-phenyl)pyrazoline}2 * 2pyridine 
• 129457-28-9 copper(II){3-(1-hydroxy-2-naphthyl)-5-(4-MeO-phenyl)pyrazoline}2 

Relevant academic research and scientific papers

Fungal metabolism of naphthoflavones

Naphthoflavones (benzoflavones) are synthetic flavonoids commonly used in drug metabolism studies as selective activators or inhibitors of cytochrome P-450 enzymes. Nowadays they are also used as a component of food supplements for body builders. There is

Efficient NIR-light emission from solid-state complexes of boron difluoride with 2′-hydroxychalcone derivatives

This article describes a series of nine complexes of boron difluoride with 2'-hydroxychacone derivatives. These dyes were synthesized very simply and exhibited intense NIR emission in the solid state. Complexation with boron was shown to impart very stron

Synthesis and complete assignment of NMR data of 20 chalcones

Chalcones, intermediates in flavonoid biosynthesis, can exhibit antibacterial, antiproliferative, and anti-inflammatory properties. Chalcones contain two benzene rings and both hydroxylated and methoxylated analogs are frequently produced by hydroxylases and O-methyltransferases in plant biosynthetic pathways. Assignments of NMR peaks in the spectra of hydroxylated and/or methoxylated chalcones can help in identifying novel chalcone derivatives isolated from natural sources by referencing these data against NMR spectra obtained from known chalcones. We report here the syntheses of 20 chalcones and complete assignments of 1H and 13C NMR spectra. Copyright