1417801-97-8

Basic information

• Product Name: 3,7-dimethoxy-6-(4-methoxy-2-(3-(phenylsulfonyl)but-3-en-1-yl)phenyl)-9,10-dihydrophenanthren-4-ol
• Synonyms: 3,7-dimethoxy-6-(4-methoxy-2-(3-(phenylsulfonyl)but-3-en-1-yl)phenyl)-9,10-dihydrophenanthren-4-ol
• CAS NO: 1417801-97-8
• Molecular Weight: 556.679
• Mol File: 1417801-97-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3,7-dimethoxy-6-(4-methoxy-2-(3-(phenylsulfonyl)but-3-en-1-yl)phenyl)-9,10-dihydrophenanthren-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,7-dimethoxy-6-(4-methoxy-2-(3-(phenylsulfonyl)but-3-en-1-yl)phenyl)-9,10-dihydrophenanthren-4-ol(1417801-97-8)
• EPA Substance Registry System: 3,7-dimethoxy-6-(4-methoxy-2-(3-(phenylsulfonyl)but-3-en-1-yl)phenyl)-9,10-dihydrophenanthren-4-ol(1417801-97-8)

Safety Data

• Hazardous Substances Data: 1417801-97-8(Hazardous Substances Data)

Upstream product

• 99615-74-4 2,4-dibromo-5-methoxylbenzaldehyde 
• 1417801-86-5 1-(benzyloxy)-5-bromo-2-methoxy-4-vinylbenzene 
• 1417801-85-4 C₁₈H₂₇BO₄ 
• 1417801-84-3 2-bromo-3-isopropoxy-4-methoxy-1-vinylbenzene 
• 591-31-1 3-methoxy-benzaldehyde 
• 40705-22-4 4-benzyloxy-6-bromo-3-methoxybenzaldehyde 
• 2973-58-2 2-bromoisovanillin 
• 1417801-94-5 1-bromo-4-methoxy-2-(3-(phenylsulfonyl)propyl)benzene 
• 1260118-78-2 1-methoxy-3-(3-(phenylsulfonyl)propyl)benzene 
• 1417801-93-4 (E)-1-methoxy-3-(3-(phenylsulfonyl)allyl)benzene 
• 65292-99-1 2-(3-methoxyphenyl)acetaldehyde 
• 1417801-90-1 5-isopropoxy-2,6-dimethoxy-9,10-dihydrophenanthren-3-yl trifluoromethanesulfonate 
• 1417801-92-3 5-isopropoxy-2,6-dimethoxy-9,10-dihydrophenanthren-3-ol 
• 1417801-91-2 3-(benzyloxy)-5-isopropoxy-2,6-dimethoxyphenanthrene 

Downstream Products

• 1417801-96-7 4-((3,7-dimethoxy-6-(4-methoxy-2-(3-(phenylsulfonyl)but-3-en-1-yl)phenyl)-9,10-dihydrophenanthren-4-yl)oxy)-2H-pyran-2-one 

Relevant articles and documents

Enantioselective and regioselective pyrone Diels-Alder reactions of vinyl sulfones: Total synthesis of (+)-cavicularin

The total synthesis of (+)-cavicularin is described. The synthesis features an enantio- and regioselective pyrone Diels-Alder reaction of a vinyl sulfone to construct the cyclophane architecture of the natural product. The Diels-Alder substrate was prepared by a regioselective one-pot three-component Suzuki reaction of a non-symmetric dibromoarene. The total synthesis of (+)-cavicularin features an enantio- and regioselective Diels-Alder reaction of a pyrone with a vinyl sulfone. The substrate for this transformation is prepared by a regioselective one-pot three-component Suzuki reaction of a non-symmetric dibromoarene.