1190085-90-5

Basic information

• Product Name: C₆₉H₉₆O₂₄
• Synonyms: C₆₉H₉₆O₂₄
• CAS NO: 1190085-90-5
• Molecular Weight: 1309.51
• Mol File: 1190085-90-5.mol

Chemical Properties

• CAS DataBase Reference: C₆₉H₉₆O₂₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₆₉H₉₆O₂₄(1190085-90-5)
• EPA Substance Registry System: C₆₉H₉₆O₂₄(1190085-90-5)

Safety Data

• Hazardous Substances Data: 1190085-90-5(Hazardous Substances Data)

Upstream product

• 1215090-31-5 C₁₃H₁₃BrO₆ 
• 1190085-94-9 C₂₃H₂₆O₁₀ 
• 1190085-88-1 C₁₇H₂₀O₇ 
• 1190085-95-0 C₂₀H₂₂O₇ 
• 1190085-92-7 C₃₁H₄₄O₁₂ 
• 1160109-58-9 C₂₂H₄₀O₄Sn 
• 20469-65-2 1-bromo-3,5-dimethoxybenzene 
• 16534-12-6 3,5-dihydroxy-4-bromobenzoic acid 
• 1041434-09-6 1-bromo-3,5-bis(methoxymethoxy)benzene 
• 350035-53-9 3,5-dihydroxy-4-bromobenzoic acid ethyl ester 
• 1190085-99-4 C₂₁H₃₁BrO₇ 
• 1190085-89-2 C₂₇H₃₆O₁₀ 

Downstream Products

• 1190085-96-1 C₆₉H₉₅BrO₂₃ 
• 1190086-00-0 C₉₃H₁₄₁N₉O₃₀ 

Relevant articles and documents

Guest-release control in enzyme-sensitive, amphiphilic-dendrimer-based nanoparticles through photochemical crosslinking

Stimuli sensitive, facially amphiphilic dendrimers have been synthesized and their enzyme-responsive nature has been determined with dual fluorescence responses of both covalently conjugated and non-covalently bound reporter units. These dual responses ar

Role of Aromatic Interactions in Temperature-Sensitive Amphiphilic Supramolecular Assemblies

Aromatic interactions were found to greatly influence the temperature-dependent dynamic behavior within supramolecular assemblies. Using an amphiphilic dendron, we systematically changed the hydrophobic groups introducing increasing levels of aromaticity while keeping the hydrophilic part constant. We show that the supramolecular assemblies become less sensitive to temperature changes when aromatic interactions in the aggregate are increased. Conversely, the absence of aromaticity in the hydrophobic moieties produces temperature-sensitive aggregates. These results show that subtle molecular-level interactions can be utilized to control temperature-sensitive behavior in the nanoscale. These findings open up new design strategies to rationally tune the behavior of stimuli-responsive supramolecular assemblies on multiple spatiotemporal scales.

Photoregulated release of noncovalent guests from dendritic amphiphilic nanocontainers

Supramolecular disassembly: Phototriggered release of noncovalently sequestered lipophilic guest molecules from dendritic supramolecular assemblies has been demonstrated. Facially amphiphilic dendrimers have been shown to provide a unique opportunity to f

Enzyme-triggered disassembly of dendrimer-based amphiphilic nanocontainers

(Figure Presented) We demonstrate a new enzyme-induced disassembly of amphiphilic nanocontainers based on dendrimers. Disassembly and the ensuing release of noncovalently bound guest molecules are of great interest because of their implications in areas s