176650-93-4

Basic information

• Product Name: 3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE
• Synonyms: 3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE
• CAS NO: 176650-93-4
• Molecular Formula: C₂₅H₂₇BrO₆
• Molecular Weight: 503.38
• Product Categories: Building Blocks for Dendrimers;Functional Materials
• Mol File: 176650-93-4.mol

Chemical Properties

• Appearance: /
• Refractive Index: 1.58
• Storage Temp.: Refrigerator
• CAS DataBase Reference: 3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE(176650-93-4)
• EPA Substance Registry System: 3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE(176650-93-4)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 176650-93-4(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research:
3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE is used as a reagent in pharmaceutical research for its ability to facilitate the synthesis of biologically active molecules. Its unique structure allows for the creation of compounds with potential therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE is used as an intermediate for the preparation of various synthetic compounds. Its versatility in chemical reactions makes it a valuable component in the development of new chemical entities.
Used in Drug Discovery and Development:
3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE is employed in drug discovery and development as a key component in the synthesis of compounds with potential pharmacological properties. Its presence in the molecular structure can influence the biological activity and therapeutic efficacy of the resulting compounds.
Used in Chemical Reactions:
3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE is utilized in various chemical reactions to modify or functionalize other molecules. Its reactivity and stability make it a suitable candidate for use in the synthesis of complex organic compounds.

InChI:InChI=1/C25H27BrO6/c1-27-20-7-18(8-21(11-20)28-2)15-31-24-5-17(14-26)6-25(13-24)32-16-19-9-22(29-3)12-23(10-19)30-4/h5-13H,14-16H2,1-4H3

Upstream product

• 877-88-3 3,5-dimethoxybenzyl bromide 
• 705-76-0 3,5-dimethoxybenzyl alcohol 
• 176650-92-3 3,5-bis(3,5-dimethoxybenzyloxy)benzyl alcohol 

Downstream Products

• 1353901-72-0 C₅₇H₅₈O₁₅ 
• 1191933-49-9 C₆₃H₆₂O₁₆ 
• 464884-88-6 bis-{3,5-bis[3,5-(dimethoxy)benzyloxy]benzyl}-dimethylammonium bromide 

Relevant articles and documents

Dendritic [2]rotaxanes: Synthesis, characterization, and properties

A series of dendritic ammonium salts have been designed and synthesized. Subsequently, they were used to construct the corresponding [2]rotaxanes by a template-directed clipping approach. Unusually, two unsymmetrical dendritic [2]rotaxanes containing fluorophore (pyrene units) were also obtained; their optical properties, such as UV/vis absorption and fluorescence, were measured. The results indicate that these two rotaxanes possess stronger intermolecular interaction in the solid state than in solution. As a result, solutions of high concentration readily formed the excimer. These special rotaxanes might be applied in dynamic fluorescence-reponsive materials, and the rotaxane structure will also be used as a strategy to adjust the aggregated behaviors of fluorescent molecules.

Dendrimer diarylethenes: The memory effect of conformation in polymer matrices

Photochromic dendrimer diarylethenes with a C-2-connected bisbenzothienylethene core were synthesized; the most notable feature of them is the strong memory effect of cyclizable conformation of the open form when generated from the closed form by visible

Chromophore-labeled dendrons as light harvesting antennae

A novel series of polyether dendrimer segments (dendrons) end-capped with pyrenyl, naphthyl, or methyl groups has been prepared by a convergent growth method. Steady-state fluorescence measurements indicate the absence of intramolecular naphthalene excimer in the naphthyl-capped dendrons. However, in the pyrenyl-capped dendrons, excimer emission predominates. Fluorescence from both the naphthyl monomer and pyrenyl excimer are quenched when a suitable electron donor (e.g., a 3-[dimethylamino]phenoxy group) is covalently attached at the dendron focal point. No sensitized emission from the dendron backbone is observed in the chromophore-labeled dendrons, although the control methyl-capped dendron fluoresces weakly at 310 nm when excited at 284 nm. Absorption and fluorescence spectra, fluorescence quantum yields, and fluorescence lifetimes for the chromophore-labeled dendrons axe reported.