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4-phenylazophenyl glycidyl ether is an organic compound with the chemical formula C15H13ClN2O. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. 4-phenylazophenyl glycidyl ether is primarily used as an intermediate in the synthesis of various dyes and pigments, particularly those with azo groups. It is also known for its potential applications in the pharmaceutical industry. Due to its chemical reactivity, it is important to handle 4-phenylazophenyl glycidyl ether with care, as it may pose health risks and environmental concerns.

3157-91-3

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3157-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3157-91-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3157-91:
(6*3)+(5*1)+(4*5)+(3*7)+(2*9)+(1*1)=83
83 % 10 = 3
So 3157-91-3 is a valid CAS Registry Number.

3157-91-3Downstream Products

3157-91-3Relevant academic research and scientific papers

Light-responsive nanocomposites combining graphene oxide with POSS based on host-guest chemistry

Teng, Zhiwei,Wang, Bingtao,Hu, Yingying,Xu, Danqian

, p. 717 - 720 (2019)

Based on the reversible host-guest inclusion/exclusion of cyclodextrin-functionalized graphene oxide (GO-CD) and azobenzene-terminated polyhedral oligomeric silsesquioxane (Azo-POSS), a novel kind of light-responsive nanocomposites GO-POSS was developed u

Multistimuli responsive polymer nanoparticles on the basis of the amphiphilic azobenzene-contained hyperbranched poly(ether amine) (hPEA-AZO)

Yu, Bing,Jiang, Xuesong,Wang, Rui,Yin, Jie

, p. 10457 - 10465 (2010)

We here reported the multistimuli responsive behavior of polymer nanoparticles, which was formed through direct dispersion of the amphiphilic azobenzene-contained hyperbranched poly(ether amine) (hPEA-AZO) in water. A series of hPEA-AZO were synthesized b

Azobenzene derivative, azobenzene derivative-containing laser anti-counterfeiting device and preparation methods of azobenzene derivative and laser anti-counterfeiting device

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Paragraph 0115; 0184; 0186; 0190; 0192; 0196; 0198, (2020/07/06)

The invention discloses an azobenzene derivative, an azobenzene derivative-containing laser anti-counterfeiting device and preparation methods of the azobenzene derivative and the laser anti-counterfeiting device. The azobenzene derivative has a structure represented by the following formula, wherein R1 and R5 are independently selected from any one of three groups defined in the specification; R2, R3, R4 and R7 are independently selected from any one of H, F, Cl, Br and CH3; and n is selected from 1-10. The anti-counterfeiting device is obtained by forming a film through thermocuring and/or ultraviolet curing, forming a sandwich structure coating layer on the surface of a substrate and then photoetching anti-counterfeiting patterns on the coating layer through a photomask. The preparationmethod of the azobenzene derivative-containing laser anti-counterfeiting device provided by the invention has the advantages of low cost, simplicity and convenience in operation, heat-resistant stability, easiness in large-scale production and the like; the laser anti-counterfeiting device prepared by the method is good in stability and high in anti-counterfeiting recognition degree, has important significance in promoting preparation of the anti-counterfeiting device, and has quite important application value in national economy and daily life of people.

Synthesis and characterization of photochromic azobenzene cellulose ethers

Li, Zhijun,Zhang, Dong,Weng, Jiabao,Chen, Biao,Liu, Haiqing

, p. 748 - 754 (2013/10/08)

Photochromic azobenzene cellulose ethers were prepared by homogeneous etherification of cellulose with 2,3-epoxypropoxy-azobenzene (EA) in N,N-dimethylacetamide/lithium chloride solution. The EA with epoxy group could highly efficiently react with cellulose to synthesize 3-azobenzyloxy-2- hydroxypropyl-cellulose (Azo-cellulose) ethers with controllable degree of substitution (DSazo). The DSazo was in a range of 0.2-2.0 adjusted by the molar ratio of EA to anhydroglucose unit of cellulose. The Azo-celluloses with DSazo ≥ 0.53 were soluble in aprotic solvents like dimethylsulfoxide. Their chemical structures and properties were characterized by elemental analysis, FT-IR, NMR, and thermogravimetric analysis. They showed reversible trans-cis-trans transition when Azo-cellulose/DMAc solutions were irradiated by successive irradiation of UV and visible light. The transition between trans- and cis- isomers could be effectively controlled by simply adjusting the irradiation time. The photo-stimulated trans-cis-trans conformational change induced conformation transition between rod-like shape of trans-isomer and skewed shape of cis-isomer.

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