176650-92-3 Usage
Uses
Used in Pharmaceutical Production:
3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL ALCOHOL is used as an active pharmaceutical ingredient for its potential therapeutic applications, leveraging its antiviral, antibacterial, and anti-inflammatory properties to develop new treatments for various diseases and conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL ALCOHOL is used as a reagent, contributing to the creation of more complex organic molecules that are essential for a wide range of industrial and research purposes.
Used in Material Development:
3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL ALCOHOL is employed as a structural component in the development of novel materials, where its unique molecular structure provides specific properties that enhance the performance of these materials.
Used in Agrochemical Manufacturing:
In the agrochemical industry, 3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL ALCOHOL is used as an intermediate in the manufacturing process, contributing to the development of effective and innovative agrochemical products.
Used in Fragrance Production:
3,5-BIS(3,5-DIMETHOXYBENZYLOXY)BENZYL ALCOHOL is also utilized in the fragrance industry, where it serves as an intermediate in the production of various scents and perfumes, adding to the complexity and uniqueness of the final product.
Check Digit Verification of cas no
The CAS Registry Mumber 176650-92-3 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 176650-92:
(8*1)+(7*7)+(6*6)+(5*6)+(4*5)+(3*0)+(2*9)+(1*2)=163
163 % 10 = 3
So 176650-92-3 is a valid CAS Registry Number.
InChI:InChI=1/C25H28O7/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/h5-13,26H,14-16H2,1-4H3
176650-92-3Relevant articles and documents
Dendrimer diarylethenes: The memory effect of conformation in polymer matrices
Fujimoto, Yuhei,Ubukata, Takashi,Yokoyama, Yasushi
supporting information; experimental part, p. 5755 - 5757 (2009/04/13)
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
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.
