1242319-83-0

Basic information

• Product Name: C₂₈H₂₅BrO₄
• Synonyms: C₂₈H₂₅BrO₄
• CAS NO: 1242319-83-0
• Molecular Weight: 505.408
• Mol File: 1242319-83-0.mol

Chemical Properties

• CAS DataBase Reference: C₂₈H₂₅BrO₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₈H₂₅BrO₄(1242319-83-0)
• EPA Substance Registry System: C₂₈H₂₅BrO₄(1242319-83-0)

Safety Data

• Hazardous Substances Data: 1242319-83-0(Hazardous Substances Data)

Upstream product

• 1144467-77-5 C₉H₁₁BrO₃ 
• 72586-64-2 ethyl 4-acetoxy-8-bromo-5-methoxy-2-naphthoate 
• 1242319-72-7 C₉H₁₀Br₂O₂ 
• 81574-69-8 2-bromo-4,6-dimethoxybenzaldehyde 
• 7507-86-0 2-bromo-5-methoxy-benzaldehyde 
• 20469-65-2 1-bromo-3,5-dimethoxybenzene 
• 100-39-0 benzyl bromide 
• 591-31-1 3-methoxy-benzaldehyde 
• 1242319-35-2 C₁₉H₁₆O₃ 
• 1242319-28-3 C₁₃H₂₀BrO₅P 

Downstream Products

• 1242319-39-6 C₄₂H₄₀O₈ 

Relevant articles and documents

SYNTHESIS OF THE POTENT IMMUNOSUPPRESSANT AGENTS DALESCONOL A AND B

This invention relates to compounds having the structure: wherein bonds α, β, γ, δ, ω, η, χ, ε, κ, and μ are each present or absent, and R1-R18 are various substituents described herein.

Total syntheses of dalesconol A and B

(Chemical equation Presented) (Chemical equation Presented) A polycyclic collapse: Use of a carefully designed acyclic intermediate participated in a cascade reaction that formed the entire core of the polyketide-derived dalesconols in a single flask (see scheme). A number of additional and carefully controlled synthetic operations completed an expeditious synthesis of both of these highly bioactive natural products as well as structural congenors.