3173-00-0

Basic information

• Product Name: 2H-1-Benzopyran-2-one, 7-methoxy-3-(4-methoxyphenyl)-
• Synonyms: 7-methoxy-3-(4-methoxyphenyl)coumarin;7-Methoxy-3-(4-methoxy-phenyl)-cumarin;4',7-dimethoxy-3-phenylcoumarin;7-methoxy-3-(4-methoxyphenyl)-chromen-2-one;7-methoxy-3-(4-methoxy-phenyl)-coumarin
• CAS NO: 3173-00-0
• Molecular Formula: C17H14O4
• Molecular Weight: 282.296
• Mol File: 3173-00-0.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 2H-1-Benzopyran-2-one, 7-methoxy-3-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-1-Benzopyran-2-one, 7-methoxy-3-(4-methoxyphenyl)-(3173-00-0)
• EPA Substance Registry System: 2H-1-Benzopyran-2-one, 7-methoxy-3-(4-methoxyphenyl)-(3173-00-0)

Safety Data

• Hazardous Substances Data: 3173-00-0(Hazardous Substances Data)

Upstream product

• 72167-80-7 3-bromo-7-methoxy-2H-chromen-2-one 
• 5720-07-0 4-methoxyphenylboronic acid 
• 531-59-9 7-methoxycoumarin 
• 673-22-3 2-Hydroxy-4-methoxybenzaldehyde 
• 100-66-3 methoxybenzene 
• 104-01-8 4-Methoxyphenylacetic acid 
• 4693-91-8 4-methoxyphenyl-acetic chloride 
• 3951-10-8 2-(4-methoxyphenyl)acetic anhydride 
• 6468-36-6 7-hydroxy-3-(4-hydroxyphenyl)-2H-chromen-2-one 
• 74-88-4 methyl iodide 
• 459-64-3 4-methoxybenzenediazonium tetrafluoroborate 
• 77-78-1 dimethyl sulfate 
• 768-60-5 4-methoxyphenylacetylen 

Downstream Products

• 1404301-54-7 7-methoxy-3-(4-methoxyphenyl)hydrocoumarin 
• 531-95-3 equol 
• 6468-37-7 3-(4-hydroxyphenyl)-7-methoxy-2H-chromen-2-one 
• 1838-44-4 2-(4-'methoxyphenyl)-6-methoxybenzo[b]furan 
• 6468-36-6 7-hydroxy-3-(4-hydroxyphenyl)-2H-chromen-2-one 
• 173676-44-3 4',7-dihydroxy-2-ethyl-isoflav-3-ene 
• 130064-36-7 2-[4-[2-(1-piperidino)-ethoxy]phenyl]-3-[4-hydroxyphenyl]-7-hydroxy-2H-1-benzopyran 
• 173676-30-7 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-chromen-2-one 
• 173676-38-5 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-naphthalen-1-yl-2H-chromene 
• 173676-53-4 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-phenoxy-2H-chromene 
• 173676-35-2 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-(4-methoxy-phenyl)-2H-chromene 
• 173676-37-4 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-(4-fluoro-phenyl)-2H-chromene 
• 173676-52-3 4-{7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2H-chromen-2-yl}-phenol 
• 173676-39-6 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-thiophen-2-yl-2H-chromene 

Relevant articles and documents

Novel coumarin compound and application thereof

The invention relates to the technical field of novel materials and organic chemicals, in particular to a novel compound, a process technology for chemically preparing the novel compound, application of the novel compound and a radiation curing formula pr

Metal-free C(3)-H arylation of coumarins promoted by catalytic amounts of 5,10,15,20-tetrakis(4-diethylaminophenyl)porphyrin

The metal-free C-H arylation of coumarins was achieved in the presence of catalytic amounts of 5,10,15,20-tetrakis(4-diethylaminophenyl)porphyrin. This mild and environmentally friendly Meerwein arylation provided facile access to a broad variety of 3-arylcoumarins in synthetically useful yields.

Palladium catalyzed dehydrogenative arylation of coumarins: An unexpected switch in regioselectivity

A new regioselective α-arylation of coumarins with unactivated simple arenes via a palladium-catalyzed twofold C-H functionalization is devised. This method offers an attractive new approach to synthesis of a wide variety of 3-arylcoumarins from readily accessible starting materials. This journal is The Royal Society of Chemistry 2013.