371258-91-2

Basic information

• Product Name: Ethanone, 1-[2-[(4-methoxyphenyl)methoxy]phenyl]-
• Synonyms: Ethanone,1-[2-[(4-methoxyphenyl)methoxy]phenyl];2'-(4-methoxybenzyloxy)acetophenone;1-{2-[(4-methoxybenzyl)oxy]phenyl}ethanone
• CAS NO: 371258-91-2
• Molecular Formula: C16H16O3
• Molecular Weight: 256.301
• Mol File: 371258-91-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[2-[(4-methoxyphenyl)methoxy]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[2-[(4-methoxyphenyl)methoxy]phenyl]-(371258-91-2)
• EPA Substance Registry System: Ethanone, 1-[2-[(4-methoxyphenyl)methoxy]phenyl]-(371258-91-2)

Safety Data

• Hazardous Substances Data: 371258-91-2(Hazardous Substances Data)

Upstream product

• 118-93-4 o-hydroxyacetophenone 
• 824-94-2 p-methoxybenzyl chloride 
• 2746-25-0 p-Methoxybenzyl bromide 

Downstream Products

• 131137-81-0 1-<2-<(4-Methoxyphenyl)methoxy>phenyl>-2-<(4-methylphenyl)sulphinyl>ethanone 
• 118-93-4 o-hydroxyacetophenone 
• 405239-74-9 tert-butyl 2-amino-4-{1-[(benzyloxy)carbonyl]-3-piperidinyl}-6-{2-[(4-methoxybenzyl)oxy]phenyl}nicotinate 
• 38276-97-0 rac-cis-2-(4-methoxyphenyl)-3-methyl-2,3-dihydrobenzofuran 
• 38276-96-9 (±)-trans-2-(4-methoxyphenyl)-3-methyl-2,3-dihydrobenzofuran 
• 726180-53-6 N-{1-[2-(4-methoxybenzyloxy)phenyl]-2-methoxymethoxyvinyl}acetamide 
• 726180-42-3 1-[2-(4-methoxybenzyloxy)phenyl]-2-methoxymethoxyethanone 
• 726180-32-1 2-hydroxy-1-[2-(4-methoxybenzyloxy)phenyl]ethanone 
• 573974-68-2 2'-(4-methoxybenzyloxy)acetophenone tosylhydrazone 

Relevant articles and documents

Tetraalkylammonium-templated stereoselective Norrish-Yang cyclization

Tetrabutylammonium salts serve as templates for the Norrish-Yang cyclization of 2-benzyloxy-acylbenzenes to give trans-dihydrobenzofuranols in high stereoselectivities. The dual cation-π interactions between an ammonium with a benzene ring and a carbonyl group play a key role in changing the conformation of the substrate, which was supported by ab initio calculations.

Synthesis and structure-activity relationships of novel IKK-β inhibitors. Part 3: Orally active anti-inflammatory agents

A series of 2-amino-3-cyano-4-alkyl-6-(2-hydroxyphenyl)pyridine derivatives was synthesized and evaluated as IκB kinase β (IKK-β) inhibitors. Modification of a novel IKK-β inhibitor 1 (IKK-β IC 50=1500nM, Cell IC50=8000nM) at the 4-p

Conjugate addition to 3-arylsulfinylchromones as a synthetic route to homochiral 2-substituted chromanones: Scope and limitations

A route to homochiral 2-substituted chromanones via the diastereoselective conjugate addition of organocopper reagents to 3-(p-tolylsulfinyl)chromones has been improved and used to prepare 2,6-dimethylchromanone (S)-4 and LL-D253α methyl ether (S)-6. The attempted preparation of a 2-phenylchromanone (flavanone) using this strategy was unsuccessful due to the lability of the intermediate 2-phenyl-3-(p-tolylsulfinyl)chromanone, which underwent sulfoxide elimination at room temperature to give the corresponding 2-phenylchromone (flavone).