85071-58-5

Basic information

• Product Name: Benzaldehyde, 2-hydroxy-3,5-dimethoxy-4-methyl-
• CAS NO: 85071-58-5
• Molecular Formula: C10H12O4
• Molecular Weight: 196.203
• Mol File: 85071-58-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-hydroxy-3,5-dimethoxy-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-hydroxy-3,5-dimethoxy-4-methyl-(85071-58-5)
• EPA Substance Registry System: Benzaldehyde, 2-hydroxy-3,5-dimethoxy-4-methyl-(85071-58-5)

Safety Data

• Hazardous Substances Data: 85071-58-5(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 19676-67-6 2,4-dimethoxy-3-methylphenol 
• 5673-07-4 2,6-dimethoxytoluene 
• 7149-92-0 2,4-dimethoxy-3-methylbenzaldehyde 
• 100-97-0 hexamethylenetetramine 

Downstream Products

• 1070888-05-9 2-(2-hydroxy-3,5-dimethoxy-4-methylphenyl)-3-methyl-6-phenethyltetrahydropyran-4-ol 
• 271578-78-0 1,3,4-trimethoxy-2-methyl-5-vinylbenzene 
• 1262943-82-7 (S)-3-(2,3,5-trimethoxy-4-methylphenyl)butan-1-ol 
• 85071-59-6 1-bromo-2,3,5-trimethoxy-4-methylbenzaldehyde 
• 100827-49-4 (2,5-dibenzyloxy-3-methoxy-4-methyl-6-nitrophenyl)acetaldehyde 
• 100827-55-2 2-methoxy-3,6-dimethyl-5-nitrohydroquinone dibenzyl ether 
• 99907-50-3 4,7-dibenzyloxy-5-methoxy-6-methylindole 
• 100827-51-8 2-methoxy-3,6-dimethylhydroquinone dibenzyl ether 
• 99892-81-6 2,3,5-trimethoxy-4-methyl-6,β-dinitrostyrene 
• 99892-80-5 2,3,5-trimethoxy-4-methyl-β-nitrostyrene 
• 2913-45-3 2-methoxy-3,6-dimethyl-1,4-benzoquinone 
• 99892-95-2 2-methoxy-3,6-dimethylhydroquinone 
• 113296-79-0 (Z)-1-acetyl-3-(2-benzyloxy-3,5-dimethoxy-4-methylphenylmethylene)-6-(2,4,5-trimethoxy-3-methylphenylmethyl)-2,5-piperazinedione 
• 113296-84-7 3-[1-(2-Benzyloxy-3,5-dimethoxy-4-methyl-phenyl)-meth-(Z)-ylidene]-6-(2,4,5-trimethoxy-3-methyl-benzyl)-piperazine-2,5-dione 

Relevant articles and documents

Broadly Applicable Stereoselective Syntheses of Serrulatane, Amphilectane Diterpenes, and Their Diastereoisomeric Congeners Using Asymmetric Hydrovinylation for Absolute Stereochemical Control

A stereogenic center, placed at an exocyclic location next to a chiral carbon in a ring to which it is attached, is a ubiquitous structural motif seen in many bioactive natural products, including di- and triterpenes and steroids. Installation of these ce

Rapid stereocontrolled assembly of the fully substituted C-aryl glycoside of kendomycin with a Prins cyclization: A formal synthesis

Prins cyclization using an electron-rich benzaldehyde and a homoallylic alcohol efficiently delivered the fully substituted C-aryl tetrahydropyranoside of kendomycin. The Royal Society of Chemistry 2006.

Synthesis of 4,7-indolequinones. The oxidative demethylation of 4,7-dimethoxyindoles with ceric ammonium nitrate

-