92831-74-8

Usage

Uses

Used in Pharmaceutical Industry:
Dihydro-4-[[3-Methoxy-4-(phenylMethoxy)phenyl]Methyl]-2(3H)-furanone is used as a key intermediate in the synthesis of biologically active ligands for pharmaceutical applications. Its unique structure allows it to interact with specific biological targets, making it a valuable component in the development of new drugs and therapeutic agents.
Used in Research and Development:
In the field of research and development, Dihydro-4-[[3-Methoxy-4-(phenylMethoxy)phenyl]Methyl]-2(3H)-furanone serves as a versatile building block for the creation of novel compounds with potential biological activity. Researchers can use Dihydro-4-[[3-Methoxy-4-(phenylMethoxy)phenyl]Methyl]-2(3H)-furanone to explore new chemical space and discover innovative molecules with therapeutic potential.
Used in Chemical Synthesis:
Dihydro-4-[[3-Methoxy-4-(phenylMethoxy)phenyl]Methyl]-2(3H)-furanone is also used in chemical synthesis processes to produce a variety of complex organic molecules. Its unique functional groups and structural features make it a valuable precursor in the synthesis of diverse chemical compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.

Upstream product

• 365423-63-8 4-(4-benzyloxy-3-methoxy-benzyl)-2-ethoxy-tetrahydro-furan 
• 927198-76-3 (+/-)-2-(4-benzyloxy-3-methoxybenzyl)butanedioic acid 1-methyl ester 
• 92831-72-6 (benzyloxy-4 methoxy-3 benzylidene)-4 dihydro-3H-furannone-2 
• 365423-60-5 1-Benzyloxy-4-[(E)-3-(2-bromo-1-ethoxy-ethoxy)-propenyl]-2-methoxy-benzene 
• 38157-08-3 (E)-3-(4-benzyloxy-3-methoxyphenyl)acrylic acid ethyl ester 
• 38153-27-4 (2E)-3-(4-O-benzyloxy-3-methoxyphenyl)prop-2-en-1-ol 
• 84755-39-5 acide (benzyloxy-4 methoxy-3 phenyl)-4 methoxycarbonyl-3 butene-3 oique 
• 121-33-5 vanillin 
• 100-44-7 benzyl chloride 
• 84755-40-8 (hydroxy-4 methoxy-3 benzyl)-4 dihydro-3H-furannone-2 

Downstream Products

• 486-29-3 (+)-lariciresinol 
• 1027237-11-1 C₃₄H₃₁⁽²⁾H₃O₆ 
• 1025906-30-2 3-(3-benzyloxy-4,5-dimethoxy-benzyl)-4-(4-benzyloxy-3-methoxy-benzyl)-dihydro-furan-2-one 
• 1027155-93-6 C₃₄H₂₉⁽²⁾H₅O₆ 
• 1026980-58-4 4-(4-benzyloxy-3-methoxy-benzyl)-3-(3,4-bis-benzyloxy-5-methoxy-benzyl)-dihydro-furan-2-one 
• 84755-40-8 (hydroxy-4 methoxy-3 benzyl)-4 dihydro-3H-furannone-2 
• 92831-77-1 benzyloxy-7 methoxy-6 (benzyloxy-4 dimethoxy-3,5 phenyl)-9 tetrahydro-3a,4,9,9a naphto<2,3-c>furannone-1 (3H) 
• 92831-80-6 (benzyloxy-4 dimethoxy-3,5 phenyl)-1-r bis-hydroxymethyl-2-t, 3-c benzyloxy-7 methoxy-6 tetrahydro-1,2,3,4 naphtalene 
• 92831-79-3 benzyloxy-7 methoxy-6 (dimethoxy-3,5 hydroxy-4 phenyl)-9 tetrahydro-3a,4,9,9a naphto<2,3-c>furannone-1 (3H) 
• 92831-81-7 (dimethoxy-3,5 hydroxy-4 phenyl)-1-r bis-hydroxymethyl-2-t, 3-c hydroxy-7 methoxy-6 tetrahydro-1,2,3,4 naphtalene 
• 92831-76-0 hydroxy-7 methoxy-6 (dimethoxy-3,5 hydroxy-4 phenyl)-9 tetrahydro-3a,4,9,9a naphto<2,3-c>furannone-1 (3H) 
• 1027570-63-3 C₃₄H₃₈⁽²⁾H₆O₇Si 
• 1027914-76-6 C₂₇H₃₂⁽²⁾H₆O₇Si 
• 1027901-10-5 4-[4-(tert-butyl-dimethyl-silanyloxy)-3-methoxy-benzyl]-3-(3,4,5-trimethoxy-benzyl)-dihydro-furan-2-one 

Relevant academic research and scientific papers

Oxidative cyclization reaction of dibenzylbutanolides with combined utilization of synthetic chemistry and biotechnological methods

We reported plant cell culture (as an enzyme source)-catalyzed oxidative cyclization reaction of dibenzylbutanolides (1a, b, d, e) to cyclic product (2a, b, d, e) via a hypothetical quinone methide intermediate.

Radical cyclisation based approach to lignans. Synthesis of 4-arylmethyldihydrofuran-2-ones

Bromoacetalisation of the cinnamyl alcohols 7a-d, obtained from the corresponding benzaldehydes, generated the bromoacetals 10a-d. The 5-exo trig radical cyclisation of the bromoacetals 10a-d followed by one step hydrolysis-oxidation of the resulting cyclic acetals 11a-d furnished the title compounds 6a-d, respectively, well-established intermediates of a variety of lignans.