356552-15-3

Basic information

• Product Name: (4-methoxyphenyl)(5-methylfuran-2-yl)methanol
• Synonyms: (4-methoxyphenyl)(5-methylfuran-2-yl)methanol
• CAS NO: 356552-15-3
• Molecular Weight: 218.252
• Mol File: 356552-15-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (4-methoxyphenyl)(5-methylfuran-2-yl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4-methoxyphenyl)(5-methylfuran-2-yl)methanol(356552-15-3)
• EPA Substance Registry System: (4-methoxyphenyl)(5-methylfuran-2-yl)methanol(356552-15-3)

Safety Data

• Hazardous Substances Data: 356552-15-3(Hazardous Substances Data)

Upstream product

• 620-02-0 5-Methylfurfural 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 104-92-7 1-bromo-4-methoxy-benzene 

Downstream Products

• 1403650-78-1 2-((4-methoxyphenyl)(prop-2-ynyloxy)methyl)-5-methylfuran 
• 21493-89-0 (4-methoxyphenyl)(5-methyl-2-furyl)methanone 
• 113386-12-2 2-<(4-Methoxyphenyl)methyl>-5-methylfuran 
• 1424149-69-8 C₁₈H₂₀O₄ 
• 1422655-96-6 3-((4-methoxyphenyl)(5-methylfuran-2-yl)methyl)pentane-2,4-dione 

Relevant articles and documents

Catalytic Formal Benzylic C-H Bond Functionalization of 2,5-Dialkylfuran Derivatives with Ferrocenyl Alcohols as Alkylation Reagents

The inert benzylic C-H bond of π-electron-rich heteroaromatic 2,5-dialkylfuran derivatives was conveniently functionalized with ferrocenyl alcohols as alkylation reagents under catalytic acidic conditions at room temperature, which features chemo- and reg

Gold catalysis: Non-spirocyclic intermediates in the conversion of furanynes by the formal insertion of an alkyne into an aryl-alkyl C-C single bond

It takes al-kynes: The formation of furyl-substituted heterocycles from furanynes with donor groups on the furan-alkyne tether and mechanistic control experiments indicate the involvement of open-chained carbenium ions in the overall insertion of an alkyne into a C-C bond, rather than the usual spirocyclic intermediates (see scheme). Copyright