54798-88-8

Basic information

• Product Name: 3-Phenyl-4-methoxy-2,5-dihydrofuran-2-one
• Synonyms: 3-Phenyl-4-methoxy-2,5-dihydrofuran-2-one;4-Methoxy-3-phenyl-2(5H)-furanone
• CAS NO: 54798-88-8
• Molecular Formula: C₁₁H₁₀O₃
• Molecular Weight: 190.2
• Mol File: 54798-88-8.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Phenyl-4-methoxy-2,5-dihydrofuran-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Phenyl-4-methoxy-2,5-dihydrofuran-2-one(54798-88-8)
• EPA Substance Registry System: 3-Phenyl-4-methoxy-2,5-dihydrofuran-2-one(54798-88-8)

Safety Data

• Hazardous Substances Data: 54798-88-8(Hazardous Substances Data)

Upstream product

• 71387-05-8 4-methoxy-3-bromo-furan-2(5H)-one 
• 98-80-6 phenylboronic acid 
• 91497-39-1 2-ethoxy-2-oxoethyl 2-phenylacetate 
• 100074-79-1 2,5-dihydro-2-oxo-3-phenyl-5-triphenylphosphoniumfuran-4-olate 
• 103-82-2 phenylacetic acid 
• 6362-63-6 ethyl 3-cyano-3-phenylpyruvate 
• 140-29-4 phenylacetonitrile 
• 56715-75-4 ethyl(3-cyano-2-methoxy)cinnamate 
• 69556-70-3 4-methoxy-5H-furan-2-one 
• 853660-88-5 5-chloro-4-methoxy-3-phenyl-2(5H)-furanone 
• 23782-85-6 3-phenyltetronic acid 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 1421237-28-6 C₂₂H₂₀FNO₄ 
• 1421237-30-0 C₂₂H₂₀FNO₄ 
• 78376-10-0 (Z)-5-benzylidene-4-hydroxy-3-phenylfuran-2(5H)-one 
• 100074-92-8 4-methoxy-3-phenyl-5-(phenylmethylene)furan-2(5H)-one 
• 1421237-20-8 C₂₂H₂₂FNO₅ 
• 100074-67-7 5-bromo-4-methoxy-3-phenylfuran-2(5H)-one 

Relevant articles and documents

Compound, as well as preparation method and application thereof

The application discloses a compound of which the structure is represented as the following formula, wherein R1 is selected from any one of F, Cl, Br, C1-C5 alkyl group, and a group having the structure as the formula (1), n = 0, 1, 2, 3, 4 or 5; the R2 is selected from any one of a group having the structure as the formula (1), a group having the structure as the formula (2), and a group having the structure as the formula (3). The compound has simple preparation method, can be used as a neuraminidase inhibitor, and has excellent antivirus activity.

An efficient procedure for the synthesis of 3-aryl-4-methoxy-2(5H)-furanones by using the microwave-promoted Suzuki-Miyaura coupling reactions

The Suzuki-Miyaura coupling reactions of 3-bromo-2(5H)-furanones with a variety of arylboronic acids, promoted by microwave heating, efficiently generate 3-aryl-2(5H)-furanones. This remarkably rapid process serves as the foundation for a simple method to

Regioselectivity control in metal hydride reductions of substituted maleic anhydrides

A systematic study of reductions of unsymmetrically substituted maleic anhydrides by a variety of metal hydride reagents indicates that the high regioselectivity observed in these reactions is controlled chiefly by electronic factors.