18064-99-8

Basic information

• Product Name: 2-(3-methoxy-phenoxy)-1-phenyl-ethanone
• Synonyms: 2-(3-methoxy-phenoxy)-1-phenyl-ethanone
• CAS NO: 18064-99-8
• Molecular Weight: 242.274
• Mol File: 18064-99-8.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2-(3-methoxy-phenoxy)-1-phenyl-ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-methoxy-phenoxy)-1-phenyl-ethanone(18064-99-8)
• EPA Substance Registry System: 2-(3-methoxy-phenoxy)-1-phenyl-ethanone(18064-99-8)

Safety Data

• Hazardous Substances Data: 18064-99-8(Hazardous Substances Data)

Upstream product

• 150-19-6 O-methylresorcine 
• 70-11-1 α-bromoacetophenone 
• 67-64-1 acetone 
• 98-86-2 acetophenone 
• 1122-95-8 sodium 4-methoxyphenolate 
• 52688-74-1 potassium 3-methoxyphenolate 

Downstream Products

• 75158-59-7 (6-methoxybenzo[b]furan-2-yl)(phenyl)methanone 
• 105243-65-0 3-chloro-2-(3-methoxyphenoxy)cinnamaldehyde 
• 105243-66-1 α-(4-formyl-3-methoxyphenoxy)acetophenone 
• 150-76-5 4-methoxy-phenol 
• 19803-06-6 2-(4-methoxyphenoxy)-1-(4-methoxyphenyl)ethan-1-one 
• 14385-49-0 8-(4'-methoxyphenoxy)acetophenone 
• 150-19-6 O-methylresorcine 
• 29556-89-6 2-(4-methoxyphenoxy)-1-phenylethan-1-ol 
• 42052-51-7 3-hydroxy-1,3-diphenylpropan-1-one 
• 29509-27-1 2-(3-methoxyphenoxy)-1-phenylethan-1-ol 
• 98-85-1 1-Phenylethanol 
• 103164-37-0 6,6'-dimethoxy-3,3'-diphenyl-[2,2']bibenzofuranyl 

Relevant articles and documents

Cleavage∕cross-coupling strategy for converting β-O-4 linkage lignin model compounds into high valued benzyl amines via dual C–O bond cleavage

Lignin is the most recalcitrant of the three components of lignocellulosic biomass. The strength and stability of the linkages have long been a great challenge for the degradation and valorization of lignin biomass to obtain bio-fuels and commercial chemicals. Up to now, the selective cleavage of C–O linkages of lignin to afford chemicals contains only C, H and O atoms. Our group has developed a cleavage/cross-coupling strategy for converting 4-O-5 linkage lignin model compounds into high value-added compounds. Herein, we present a palladium-catalyzed cleavage/cross-coupling of the β-O-4 lignin model compounds with amines via dual C–O bond cleavage for the preparation of benzyl amine compounds and phenols.

Facile synthesis of 3-aryl benzofurans, 3-aryl benzothiophenes, 2-aryl indoles and their dimers

The preparation of 3-aryl benzofuran and benzothiophenes and their dimers at 2-position and, 2-aryl indoles and their 3-position dimers preparation is described.

Efficient synthetic approach to substituted benzo[b]furans and benzo[b]thiophenes by iodine-promoted cyclization of enaminones

An efficient synthetic approach to the substituted benzo[b]furan and benzo[b]thiophene scaffolds by iodine-mediated cyclization of the corresponding enaminones is described. This protocol was applied to a large series of these latter precursors to afford the respective benzoheterocycles substituted at the C-2 position by a carbonyl group functionality. A study of the factors that control this process reveals that the reactivity depends on the presence of electron-donor groups in the aryl ring of the aryloxycarbonylic and arylthiocarbonylic moieties.