391278-03-8

Basic information

• Product Name: C₃₂H₄₀O₇
• Synonyms: C₃₂H₄₀O₇
• CAS NO: 391278-03-8
• Molecular Weight: 536.665
• Mol File: 391278-03-8.mol

Chemical Properties

• CAS DataBase Reference: C₃₂H₄₀O₇(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₂H₄₀O₇(391278-03-8)
• EPA Substance Registry System: C₃₂H₄₀O₇(391278-03-8)

Safety Data

• Hazardous Substances Data: 391278-03-8(Hazardous Substances Data)

Upstream product

• 391277-98-8 C₁₇H₂₆O₅ 
• 391277-97-7 C₁₆H₂₆O₆ 
• 391277-96-6 C₁₆H₂₆O₅ 
• 391277-99-9 C₁₇H₂₆O₆ 
• 391278-00-5 C₁₇H₂₆O₆ 
• 391278-10-7 C₁₉H₃₀O₆ 
• 391278-01-6 C₁₉H₃₀O₆ 
• 391278-12-9 C₂₃H₄₀O₅Si 
• 391277-95-5 C₁₇H₂₆O₂ 
• 1053640-16-6 C₂₂H₃₈O₆Si 
• 1027036-06-1 C₂₀H₃₄O₆Si 
• 391278-11-8 C₁₇H₂₈O₅ 
• 100-39-0 benzyl bromide 
• 391278-09-4 6.8ac-Dimethyl-3c-isopropenyl-Δ⁶-(4arH)-octalon-(1) 

Downstream Products

• 790664-57-2 C₁₈H₂₈O₇ 
• 391278-04-9 C₂₅H₃₄O₇ 
• 391278-07-2 C₂₅H₃₄O₆ 
• 391278-05-0 C₂₅H₃₆O₇ 
• 391278-06-1 C₂₆H₃₈O₉S 

Relevant articles and documents

A synthetic approach toward taxol analogs: Studies on the construction of the CD ring

Tricycle 6, containing the CD ring of taxol, is constructed from (S)-(+)-carvone in 21 steps involving a Diels-Alder reaction with isoprene, a Baeyer-Villiger oxidation, an Oppenaurer oxidation and Meerwein-Ponndorf-Verley reduction, a stereospecific Grig

Synthesis of the CD ring in taxol from (S)-(+)-carvone

The tricycle 16 containing a functionalized CD ring is constructed from (S)-(+)-carvone in 21 steps involving a Baeyer-Villiger oxidation, an Oppenaurer oxidation and Meerwein-Ponndorf-Verley reduction, a stereospecific Grignard addition, and an intramole