95316-34-0

Basic information

• Product Name: 3-Hydroxy-1-methoxy-2-(2-methoxy-phenoxy)-1-(4-hydroxy-3-methoxy-phenyl)-propan
• Synonyms: 3-Hydroxy-1-methoxy-2-(2-methoxy-phenoxy)-1-(4-hydroxy-3-methoxy-phenyl)-propan
• CAS NO: 95316-34-0
• Molecular Weight: 334.369
• Mol File: 95316-34-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Hydroxy-1-methoxy-2-(2-methoxy-phenoxy)-1-(4-hydroxy-3-methoxy-phenyl)-propan(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Hydroxy-1-methoxy-2-(2-methoxy-phenoxy)-1-(4-hydroxy-3-methoxy-phenyl)-propan(95316-34-0)
• EPA Substance Registry System: 3-Hydroxy-1-methoxy-2-(2-methoxy-phenoxy)-1-(4-hydroxy-3-methoxy-phenyl)-propan(95316-34-0)

Safety Data

• Hazardous Substances Data: 95316-34-0(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 7382-59-4 guaiacylglycerol-β-guaiacyl ether 
• 36382-86-2 4-[3-Hydroxy-2-(2-methoxy-phenoxy)-prop-(Z)-ylidene]-2-methoxy-cyclohexa-2,5-dienone 

Downstream Products

• 97-54-1 2-methoxy-4-propenylphenol 
• 90-05-1 2-methoxy-phenol 
• 2785-87-7 2-methoxy-4-n-propylphenol 
• 2305-13-7 3-Guaiacylpropanol 

Relevant articles and documents

High Yield Production of Natural Phenolic Alcohols from Woody Biomass Using a Nickel-Based Catalyst

Efficient depolymerization of woody biomass to produce natural phenolic alcohols not only preserves the original structure of lignin, but also makes the depolymerization process atom-efficient. Here, high yield production of natural phenolic alcohols (38.7 wt %) from woody biomass has been achieved using a Ni/C catalyst in a methanol–water co-solvent. The Ni-based catalyst can efficiently etherify the Cα?OH group in lignin β-O-4 motifs under hydrogen atmosphere, which can break the hydrogen bond between the Cβ?O oxygen and the Cα?OH proton to facilitate the Cβ?O cleavage. It was reported that water can also accelerate the etherification of raw lignin with methanol through in situ formation of acid. Our results suggest that breaking the intramolecular hydrogen bonds can accelerate the Cβ?O cleavage, keeping the original structure of lignin unchanged. This work highlights the significance of structure modification in lignin depolymerization and displays a clear potential for the valorization of whole biomass.

Are quinone methides responsible for yellowing of paper in light?

Irradiation of tetrahydrofuran solutions of quinone methide 1 at 350 nm resulted in the formation of yellow oligomeric products and guaiacol. The rate constants determined for the disappearance of the starting compound and those of guaiacol formation show