1220498-60-1

Basic information

• Product Name: 1-tetrahydropyran-2''-yloxy-4-(2',6'-dimethoxyphenyl)-naphthalene
• Synonyms: 1-tetrahydropyran-2''-yloxy-4-(2',6'-dimethoxyphenyl)-naphthalene
• CAS NO: 1220498-60-1
• Molecular Weight: 364.441
• Mol File: 1220498-60-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-tetrahydropyran-2''-yloxy-4-(2',6'-dimethoxyphenyl)-naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-tetrahydropyran-2''-yloxy-4-(2',6'-dimethoxyphenyl)-naphthalene(1220498-60-1)
• EPA Substance Registry System: 1-tetrahydropyran-2''-yloxy-4-(2',6'-dimethoxyphenyl)-naphthalene(1220498-60-1)

Safety Data

• Hazardous Substances Data: 1220498-60-1(Hazardous Substances Data)

Upstream product

• 851231-30-6 1,3-dimethoxy-2-(4',4',5',5'-tetramethyl-1',3',2'-dioxaborolanyl)-benzene 
• 70654-65-8 1‐tetrahydropyran‐2’‐yloxy‐4‐bromonaphthalene 

Relevant articles and documents

Enantioselective synthesis of (+)-estrone exploiting a hydrogen bond-promoted Diels?Alder reaction

Starting from Danes diene and methylcyclopentenedione, (+)-estrone is synthesized along the Quinkert?Dane route in 24% total yield. The key step is an enantioselective Diels?Alder reaction promoted by an amidinium catalyst as efficiently as by a traditional Ti-TADDOLate Lewis acid.