98751-47-4

Basic information

• Product Name: 1-Propanone, 1-(4-ethoxy-3-methoxyphenyl)-2,3-dihydroxy-
• CAS NO: 98751-47-4
• Molecular Formula: C12H16O5
• Molecular Weight: 240.256
• Mol File: 98751-47-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 1-(4-ethoxy-3-methoxyphenyl)-2,3-dihydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 1-(4-ethoxy-3-methoxyphenyl)-2,3-dihydroxy-(98751-47-4)
• EPA Substance Registry System: 1-Propanone, 1-(4-ethoxy-3-methoxyphenyl)-2,3-dihydroxy-(98751-47-4)

Safety Data

• Hazardous Substances Data: 98751-47-4(Hazardous Substances Data)

Upstream product

• 1835-11-6 4-benzyloxy-3-methoxyacetophenone 
• 77891-26-0 1-(4-ethoxy-3-methoxyphenyl)propane-1,2,3-triol 
• 186255-41-4 1-(4-ethoxy-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethanone 
• 498-02-2 1-(3-methoxy-4-hydroxyphenyl)ethanone 
• 84159-64-8 4-ethoxy-3-methoxybromoacetylbenzene 
• 75665-89-3 1-<(4-ethoxy-3-methoxy)phenyl>ethan-1-one 
• 22317-29-9 1-(4-(benzyloxy)-3-methoxyphenyl)-2-(2-methoxyphenoxy)ethan-1-one 
• 1835-12-7 3-methoxy-4-benzyloxy-α-bromoacetophenone 
• 22317-34-6 β-hydroxy-α-(2-methoxyphenoxy)4-hydroxy-3-methoxypropiophenone 
• 7382-59-4 guaiacylglycerol-β-guaiacyl ether 
• 77891-30-6 1-(4-ethoxy-3-methoxyphenyl)-3-hydroxy-2-(2-methoxyphenoxy)propan-1-one 

Relevant articles and documents

Role of laccase as an enzymatic pretreatment method to improve lignocellulosic saccharification

The recalcitrant nature of lignocellulose, in particular due to the presence of lignin, is found to decrease the efficiency of cellulases during the saccharification of biomass. The efficient and cost effective removal of lignin is currently a critical bi

Singlet oxygen in the photodegradation of lignin models

The photochemical oxidation of lignin models in the presence of singlet oxygen was studied. The treatment of the non-phenolic β-O-4 aryl ether derivatives 6, 7, and 8 in the presence of both oxygen and Rose Bengal gave products deriving from a formal β-C-O cleavage formation. By this way. the derivatives 12, 13, and 15 were obtained. The photochemical oxidation of the phenolic β-O-4 aryl ether 9 gave the same type of product confirming that, in this case, the presence of the carbonyl group is not indispensable to have the cleavage reaction. The use of the model compound 10 showed that, when the phenoxy part of the molecule shows a lower reactivity towards singlet oxygen, the oxidation of the phenol moiety to hydroquinone call occur. The photochemical behaviour of these model compounds can be rationalised from a reaction of singlet oxygen with the phenoxy part of the molecule.