622852-28-2

Basic information

• Product Name: 2,5-dihydroxy-4-methoxy-3-methyl-benzaldehyde
• Synonyms: 2,5-dihydroxy-4-methoxy-3-methyl-benzaldehyde
• CAS NO: 622852-28-2
• Molecular Weight: 182.176
• Mol File: 622852-28-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,5-dihydroxy-4-methoxy-3-methyl-benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-dihydroxy-4-methoxy-3-methyl-benzaldehyde(622852-28-2)
• EPA Substance Registry System: 2,5-dihydroxy-4-methoxy-3-methyl-benzaldehyde(622852-28-2)

Safety Data

• Hazardous Substances Data: 622852-28-2(Hazardous Substances Data)

Upstream product

• 1760-80-1 2-methoxy-3-methylbenzene-1,4-diol 
• 777858-58-9 2-methoxy-1,4-bis(methoxymethoxy)-3-methylbenzene 
• 25576-97-0 2,3,6-trimethoxytoluene 
• 761457-29-8 1-bromo-4-methoxy-2,5-bis(methoxymethoxy)-3-methylbenzene 
• 96502-90-8 acetic acid 2,4-dimethoxy-3-methyl-phenyl ester 
• 5673-07-4 2,6-dimethoxytoluene 
• 19676-67-6 2,4-dimethoxy-3-methylphenol 
• 2207-57-0 2-methoxy-3-methyl-1,4-benzoquinone 
• 60512-80-3 2′,4′-dimethoxy-3′-methylacetophenone 

Downstream Products

• 808766-02-1 [2-((1S,3S)-4-Benzyloxy-1,3-dimethyl-butyl)-6-methoxy-7-methyl-benzofuran-5-yloxy]-tert-butyl-dimethyl-silane 
• 808765-99-3 4-(tert-butyl-dimethyl-silanyloxy)-6-hydroxymethyl-3-methoxy-2-methyl-phenol 
• 183202-73-5 (5R,6R,7S,8R,9R,12S,13E,16S,18S,19S)-6,7,8,9,10,11,12,15,16,17,18,19-dodecahydro-4,7,19-trihydroxy-2,6,8,12,14,16,18-heptamethyl-1,19:5,9-diepoxybenzo[18]annulen-3(5H)-one 
• 808766-15-6 5-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-4-methoxy-3-methyl-benzaldehyde 

Relevant articles and documents

Synthesis of polyfluoroalkyl aza-polycyclic aromatic hydrocarbons enabled by addition of perfluoroalkyl radicals onto vinyl azides

Radical perfluoroalkylation of α-(biaryl-2-yl)vinyl azides is capable of supplying polyfluoroalkyl aza-polycyclic aromatic hydrocarbons (aza-PAHs). Commercially available Me3SiRf (Rf = CF 3, C2F5

Access to orthogonal protected phenols - Synthesis of a silylated quinol

Herein we describe the synthesis of t-butyldimethylsilyl protected quinol (9), using an oxidation/reduction sequence to create the desired orthogonality. The title compound acts as a synthetic equivalent for a quinone, required in the total synthesis of E