92831-76-0

Basic information

• Product Name: hydroxy-7 methoxy-6 (dimethoxy-3,5 hydroxy-4 phenyl)-9 tetrahydro-3a,4,9,9a naphto<2,3-c>furannone-1 (3H)
• CAS NO: 92831-76-0
• Molecular Weight: 386.401
• Mol File: 92831-76-0.mol

Chemical Properties

• CAS DataBase Reference: hydroxy-7 methoxy-6 (dimethoxy-3,5 hydroxy-4 phenyl)-9 tetrahydro-3a,4,9,9a naphto<2,3-c>furannone-1 (3H)(CAS DataBase Reference)
• NIST Chemistry Reference: hydroxy-7 methoxy-6 (dimethoxy-3,5 hydroxy-4 phenyl)-9 tetrahydro-3a,4,9,9a naphto<2,3-c>furannone-1 (3H)(92831-76-0)
• EPA Substance Registry System: hydroxy-7 methoxy-6 (dimethoxy-3,5 hydroxy-4 phenyl)-9 tetrahydro-3a,4,9,9a naphto<2,3-c>furannone-1 (3H)(92831-76-0)

Safety Data

• Hazardous Substances Data: 92831-76-0(Hazardous Substances Data)

Upstream product

• 84755-40-8 (hydroxy-4 methoxy-3 benzyl)-4 dihydro-3H-furannone-2 
• 84755-39-5 acide (benzyloxy-4 methoxy-3 phenyl)-4 methoxycarbonyl-3 butene-3 oique 
• 92831-74-8 4-<<4-(benzyloxy)-3-methoxyphenyl>methyl>dihydro-2(3H)-furanone 
• 92831-72-6 (benzyloxy-4 methoxy-3 benzylidene)-4 dihydro-3H-furannone-2 
• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 6512-67-0 (+/-)-trans-2-(3,5-dimethoxy-4-hydroxybenzyl)-3-(4-hydroxy-3-methoxybenzyl)-butanolide 
• 92831-75-9 <(benzyloxy-4 dimethoxy-3,5 phenyl) hydroxymethyl>-3 (benzyloxy-4 methoxy-3 benzyl)-4 dihydro-3H-furannone-2 

Downstream Products

• 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 
• 92831-81-7 (dimethoxy-3,5 hydroxy-4 phenyl)-1-r bis-hydroxymethyl-2-t, 3-c hydroxy-7 methoxy-6 tetrahydro-1,2,3,4 naphtalene 
• 92831-77-1 benzyloxy-7 methoxy-6 (benzyloxy-4 dimethoxy-3,5 phenyl)-9 tetrahydro-3a,4,9,9a naphto<2,3-c>furannone-1 (3H) 

Relevant articles and documents

Establishment of Camellia sinensis cell culture with high peroxidase activity and oxidative coupling reaction of dibenzylbutanolides

We succeeded in establishment of Camellia sinensis cell culture with high peroxidase activity. When dibenzylbutanolides (1a-c) were reacted with C. sinensis cell culture, peroxidase-catalyzed oxidative coupling of 1a-c to cyclic products (2a-c) proceeded

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.