73663-56-6

Basic information

• Product Name: (3,4-Dimethoxy-phenyl)-[5-(3,4-dimethoxy-phenyl)-oxazol-2-yl]-methanol
• Synonyms: (3,4-Dimethoxy-phenyl)-[5-(3,4-dimethoxy-phenyl)-oxazol-2-yl]-methanol
• CAS NO: 73663-56-6
• Molecular Weight: 371.39
• Mol File: 73663-56-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3,4-Dimethoxy-phenyl)-[5-(3,4-dimethoxy-phenyl)-oxazol-2-yl]-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (3,4-Dimethoxy-phenyl)-[5-(3,4-dimethoxy-phenyl)-oxazol-2-yl]-methanol(73663-56-6)
• EPA Substance Registry System: (3,4-Dimethoxy-phenyl)-[5-(3,4-dimethoxy-phenyl)-oxazol-2-yl]-methanol(73663-56-6)

Safety Data

• Hazardous Substances Data: 73663-56-6(Hazardous Substances Data)

Upstream product

• 73663-61-3 5-(3,4-Dimethoxyphenyl)oxazole 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 73663-58-8 2-(3,4-dimethoxybenzyl)-5-(3,4-dimethoxyphenyl)oxazole 
• 32407-68-4 2-(3,4-Dimethoxy-phenyl)-N-[2-(3,4-dimethoxy-phenyl)-ethyl]-2-hydroxy-acetamide 
• 139-76-4 N-(3,4-dimethoxyphenethyl)-2-(3,4-dimethoxyphenyl)acetamide 

Relevant articles and documents

Oxazoles in Organic Chemistry. 2. Application to the Synthesis of Benzylisoquinoline Alkaloids

A conceptually new route to the benzylisoquinoline alkaloids has been devised.The reaction of 2-lithiooxazoles with aromatic aldehydes to generate the thermodynamically favored 2-substituted oxazoles constitutes the key step in this process.A single-pot two carbon-carbon bond-joining reaction leading to an oxazoline suitable for further transformation to a phenethylamide is also described.