313344-25-1

Basic information

• Product Name: 2-[4-(benzyloxy)phenylmethyl]furan
• Synonyms: 2-[4-(benzyloxy)phenylmethyl]furan
• CAS NO: 313344-25-1
• Molecular Weight: 264.324
• Mol File: 313344-25-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-[4-(benzyloxy)phenylmethyl]furan(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[4-(benzyloxy)phenylmethyl]furan(313344-25-1)
• EPA Substance Registry System: 2-[4-(benzyloxy)phenylmethyl]furan(313344-25-1)

Safety Data

• Hazardous Substances Data: 313344-25-1(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 5544-60-5 4-(benzyloxy)benzyl bromide 
• 110-00-9 furan 
• 66646-88-6 (E)-N-benzylideneglycine methyl ester 
• 103-71-9 phenyl isocyanate 
• 395649-41-9 methyl (E)-2-(benzylideneamino)propanoate 
• 934744-85-1 C₂₄H₂₂O₆ 
• 67628-17-5 (S)-{[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-amino}-phenyl-acetic acid methyl ester 
• 53933-42-9 2-(benzylidene-amino)-propionic acid methyl ester 
• 66646-88-6 methyl 2-(benzylideneamino)acetate 
• 13803-83-3 methyl (S)-2-(benzylideneamino)-3-methylbutanoate 
• 7517-19-3 methyl (L)-leucinate hydrochloride 
• 100-52-7 benzaldehyde 
• 75691-28-0 methyl (S)-2-(benzylideneamino)-4-methylpentanoate 

Downstream Products

• 66123-90-8 4-(fur-2-ylmethyl)phenol 

Relevant articles and documents

Solid phase Diels-Alder/retro Diels-Alder reactions. A new method for traceless linker strategy

A resin-bound furan has been efficiently synthesized from Merrifield resin. This new polymer reacts with an acetylenic dienophile to afford a thermally stable Diels-Alder adduct. Transformation of the adduct by Michael reaction with thiophenol has allowed an easy retro Diels-Alder reaction. This 'safety-catch' procedure leads to the formation of a chemically and stereochemically pure alkene and to the regeneration of the polymer-bound furan. (C) 2000 Elsevier Science Ltd.

Stereoselective 1,3-dipolar cycloaddition of a maleate derivative with azomethine ylides derived from α-amino esters: Synthesis of 3-pyrrolines

A new preparation of 3-pyrrolines is described by [3+2] cycloadditions of N-metalated azomethine ylides derived from α-amino esters with a dimethyl 7-oxabicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylate derivative, followed by retro-Diels-Alder reactions. T