72536-33-5

Basic information

• Product Name: 4,8-dihydroxypinoresinol
• CAS NO: 72536-33-5
• Molecular Weight: 390.39
• Mol File: 72536-33-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4,8-dihydroxypinoresinol(CAS DataBase Reference)
• NIST Chemistry Reference: 4,8-dihydroxypinoresinol(72536-33-5)
• EPA Substance Registry System: 4,8-dihydroxypinoresinol(72536-33-5)

Safety Data

• Hazardous Substances Data: 72536-33-5(Hazardous Substances Data)

Upstream product

• 1135-24-6 3-(4-hydroxy-3-methoxyphenyl)acrylic acid 
• 458-35-5 coniferol 
• 77550-11-9 4-cis,8-cis-bis(4-hydroxy-3-methoxyphenyl)-3,7-dioxabicyclo<3.3.0>octane-2,6-dione 
• 38209-42-6 threo-2,3-bis-(α-hydroxy-4-hydroxy-3-methoxybenzyl)butane-1,4-diol 
• 72536-37-9 4,8-dimethoxypinoresinol 
• 1135-24-6 (E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid 
• 63281-70-9 2,6-bis-(4-acetoxy-3-methoxyphenyl)-3,7-dioxabicyclo<3.3.0>octane-4,8-dione 

Downstream Products

• 81902-89-8 4,8-diethoxypinoresinol 
• 69854-19-9 2,6-bis-(3,4-dimethoxyphenyl)-3,7-dioxabicyclo<3.3.0>octane-4,8-dione 
• 38209-42-6 threo-2,3-bis-(α-hydroxy-4-hydroxy-3-methoxybenzyl)butane-1,4-diol 
• 72536-39-1 threo-2,3-bis-(α-hydroxy-3,4-dimethoxybenzyl)butane-1,4-diol 
• 72536-34-6 4,8-dihydroxyeudesmin 
• 63281-70-9 2,6-bis-(4-acetoxy-3-methoxyphenyl)-3,7-dioxabicyclo<3.3.0>octane-4,8-dione 
• 72536-36-8 4,8-diacetoxyeudesmin 
• 81902-90-1 4,8-dimethoxypinoresinol diacetate 
• 72536-42-6 C₃₆H₃₈O₁₂S₂ 
• 487-36-5 (+/-)-epipinoresinol 
• 487-36-5 (+/-)-pinoresinol 
• 526-06-7 (+/-)-dimethylpinoresinol 
• 72536-41-5 4,8-bistosyloxypinoresinol ditosylate 
• 92116-30-8 2,6-exo-bis(3-methoxy-4-tosyloxyphenyl)-4,8-exo-dihydroxy-3,7-dioxabicyclo<3.3.0>octane 

Relevant articles and documents

Synthesis and 1H N.M.R. Spectroscopic Analysis of Some 3,7-Dioxabicyclooctane Lignans

Within the framework of a synthetic project towards the preparation of the natural germination inhibitor 2,6-diaryl-3,7-dioxabicyclooctane, several molecules with the same bicyclic skeleton were prepared and their 1H n.m.r. spectra are described in detail.For the symmetrical systems particularly, the spectra exhibited second-order features and were interpreted analytically or, when necessary, by computer simulation.These n.m.r. data enabled a conformational analysis of the ring system.