80067-55-6

Basic information

• Product Name: 2-ethyl-4,5-dimethoxy-benzaldehyde
• CAS NO: 80067-55-6
• Molecular Weight: 194.23
• Mol File: 80067-55-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-ethyl-4,5-dimethoxy-benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ethyl-4,5-dimethoxy-benzaldehyde(80067-55-6)
• EPA Substance Registry System: 2-ethyl-4,5-dimethoxy-benzaldehyde(80067-55-6)

Safety Data

• Hazardous Substances Data: 80067-55-6(Hazardous Substances Data)

Upstream product

• 5392-10-9 2-bromo-4,5-dimethoxybenzaldehyde 
• 52095-39-3 2-ethenyl-4,5-dimethoxybenzaldehyde 
• 67-66-3 chloroform 
• 10028-15-6 ozone 
• 5888-51-7 4-ethylveratrole 
• 7647-01-0 hydrogenchloride 
• 7446-70-0 aluminium trichloride 
• 74-90-8 hydrogen cyanide 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 80067-41-0 ethyl-2,4-diacetyl-3-(2-ethyl-4,5-dimethoxyphenyl)-glutarate 
• 56183-33-6 2-ethyl-4,5-dimethoxy-benzoic acid 
• 408308-73-6 3-(2-ethyl-4,5-dimethoxy-phenyl)-2-cyano-propionic acid ethyl ester 
• 101268-54-6 3-(2-ethyl-4,5-dimethoxy-phenyl)-propionic acid 
• 80067-44-3 β-(2-ethyl-4,5-dimethoxyphenyl)-glutaric acid 
• 80067-50-1 β-(2-ethyl-4,5-dimethoxyphenyl)-N-methylglutarimide 
• 80067-47-6 β-(2-ethyl-4,5-dimethoxyphenyl)-glutaric anhydride 
• 757237-97-1 2-ethyl-4,5-dimethoxyphenol 
• 577-68-4 m-hemipinic acid 
• 34582-24-6 4-(2-ethyl-4,5-dimethoxy-benzylidene)-2-phenyl-4H-oxazol-5-one 

Relevant articles and documents

Enantioselective Remote C(sp3)-H Cyanation via Dual Photoredox and Copper Catalysis

The remote C(sp3)-H cyanation of carboxamides has been described by merging photoredox and copper catalysis in a site-selective and enantiocontrolled manner. The protocol is the integration of photoinduced and nitrogen-centered radical-mediated intermolecular hydrogen atom transfer with chiral copper-complex-catalyzed radical cyanation. This strategy gives enantio-enriched cyanated amides in high yields.

6-alkyl derivatives of 3-(3,4-dihydroxyphenyl)alanine (Dopa). I. Synthesis via oxazolinones.

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