176650-93-4 Usage
Description
3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE is a chemical compound that belongs to the family of benzyl bromides. It is characterized by the presence of two 3,5-dimethoxybenzyloxy groups attached to a benzyl bromide moiety. 3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE is commonly used in organic synthesis and chemical reactions, particularly in the field of pharmaceutical research. It is often utilized as a reagent or intermediate in the preparation of various biologically active molecules, as well as in the production of synthetic compounds with potential pharmacological properties. 3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL BROMIDE has garnered interest in the scientific community due to its versatile applications and potential contributions to drug discovery and development.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 176650-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,6,5 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 176650-93:
(8*1)+(7*7)+(6*6)+(5*6)+(4*5)+(3*0)+(2*9)+(1*3)=164
164 % 10 = 4
So 176650-93-4 is a valid CAS Registry Number.
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
176650-93-4Relevant articles and documents
Dendritic [2]rotaxanes: Synthesis, characterization, and properties
Liu, Guoxing,Li, Ziyong,Wu, Di,Xue, Wen,Li, Tingting,Liu, Sheng Hua,Yin, Jun
, p. 643 - 652 (2014/04/03)
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.
Chromophore-labeled dendrons as light harvesting antennae
Stewart, Gina M.,Fox, Marye Anne
, p. 4354 - 4360 (2007/10/03)
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.
