51559-36-5

Basic information

• Product Name: 5-METHOXYCOUMARIN
• Synonyms: 5-METHOXYCOUMARIN;5-METHOXY-2H-CHROMEN-2-ONE
• CAS NO: 51559-36-5
• Molecular Formula: C₁₀H₈O₃
• Molecular Weight: 176.17
• Mol File: 51559-36-5.mol
• Article Data: 14

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-METHOXYCOUMARIN(CAS DataBase Reference)
• NIST Chemistry Reference: 5-METHOXYCOUMARIN(51559-36-5)
• EPA Substance Registry System: 5-METHOXYCOUMARIN(51559-36-5)

Safety Data

• Hazardous Substances Data: 51559-36-5(Hazardous Substances Data)

Upstream product

• 5451-83-2 acetic acid 3-methoxyphenyl ester 
• 1279587-02-8 3-methoxyphenyl (2E)-3-(dimethylamino)prop-2-enoate 
• 150-19-6 O-methylresorcine 
• 186581-53-3 diazomethane 
• 6093-67-0 5-hydroxycoumarin 
• 471-25-0 Propiolic acid 
• 623-47-2 propynoic acid ethyl ester 
• 105786-78-5 3-Ethoxyacrylsaeure-3-methoxyphenylester 
• 85995-43-3 methyl 2-chloro-6-methoxy-cis-cinnamate 
• 617-48-1 malic acid 
• 74-88-4 methyl iodide 

Downstream Products

• 38489-79-1 (E)-3-(2-hydroxy-6-methoxyphenyl)acrylic acid 
• 38489-75-7 2,6-dimethoxy-cis-cinnamic acid 
• 6093-67-0 5-hydroxycoumarin 
• 208993-91-3 3-(R)-(2-Hydroxy-6-methoxy)phenyl-4-(S)-hydroxymethyl-N-(R)-α-methylbenzyl-pyrrolidine 
• 85995-45-5 methyl 2,6-dimethoxy-cis-cinnamate 
• 749879-26-3 3-(2-hydroxy-6-methoxy-phenyl)-propionic acid 

Relevant articles and documents

13C NMR Spectral Studies of Some Methoxycoumarin Derivatives. A Re-assignment for Citropten (Limettin) and an Examination of Peri-Proximity Effects for the Methyl-Methoxy and Methoxy-Methyl Couples

The 13C chemical shifts and 13C-1H coupling constants of some methoxycoumarins are reported.Some earlier spectral assignments, including those for citropten (limettin), require revision.Methoxy substituent effects on long-range 13C-1H couplings in coumarins are highlighted.Peri-proximity effects for the methyl-methoxy and mehoxy-methyl couples are derived, and the value of these effects in the assignment of peri-substituted compounds is illustrated. KEY WORDS 13C NMR Methoxycoumarins Citropten Limettin 13C-1H coupling constant Peri-proximity effects

Process for preparing coumarin derivatives using phenol and propiolic acid

Provided is a manufacturing method of coumarin derivative. The manufacturing method of coumarin derivative comprises a step of making a phenol compound react with a propiolic acid compound. According to the present invention, the manufacturing method of coumarin derivative is quick and efficient, and is useful to fields requiring synthesis of coumarin derivatives of various structures.COPYRIGHT KIPO 2016

Improved synthesis of coumarins by iron(III)-catalyzed cascade reaction of propiolic acids and phenols

The reaction of propiolic acids with phenols in the presence of FeClAgOTf catalyst proceeded efficiently in a mixed solvent of trifluoroacetic acid and 1,2-dichloroethane, and provided coumarins in good to high yields. This iron-catalyzed reaction offers a much-improved synthesis of coumarins. Thieme Stuttgart New York.