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2,2,4-trimethyl-5-phenylfuran-3(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103595-95-5

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103595-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103595-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,9 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103595-95:
(8*1)+(7*0)+(6*3)+(5*5)+(4*9)+(3*5)+(2*9)+(1*5)=125
125 % 10 = 5
So 103595-95-5 is a valid CAS Registry Number.

103595-95-5Downstream Products

103595-95-5Relevant academic research and scientific papers

Acid-catalyzed decomposition and stability of diazofuranones: Experimental and mechanistic study

Semenok, Dmitrii,Mereshchenko, Andrey S.,Medvedev, Jury,Visentin, Giorgio

, (2019/12/15)

Reactions of substituted 4-diazotetrahydrofurane-3-ones with various acids (pKa 2 + cation was confirmed by density functional theory (DFT) calculations at the PBE0/6-31+G(d) functional due to good agreement between calculated and experimental data on the acid stability of diazoketones in different solvents.

A New Powerful Approach to Multi-Substituted 3(2H)-Furanones via Br?nsted Acid-Catalyzed Reactions of 4-Diazodihydrofuran-3-ones

Medvedev, Jury J.,Semenok, Dmitrii V.,Azarova, Xenia V.,Rodina, Liudmila L.,Nikolaev, Valerij A.

, p. 4525 - 4532 (2016/12/14)

The interaction of 5,5-dialkyl(diaryl)-substituted 4-diazo-3(2H)furanones with Br?nsted acids (TFA, TsOH, etc.) causes elimination of nitrogen accompanied by 1,2-nucleophilic rearrangement, giving rise to exclusive formation of 4,5-dialkyl(diaryl)-substit

Photoreaction of 1-Aryl 1,3-Diketones. Trapping Reaction of the Biradicals Generated in the Type II Reaction with Oxygen

Yoshioka, Michikazu,Funayama, Kazuhiko,Hasegawa, Tadashi

, p. 1411 - 1414 (2007/10/02)

The biradicals generated in the type II photoreaction of 1-aryl-2,4-dimethylpentane-1,3-diones (1) were trapped by oxygen to form biradical-oxygen complexes.In acetonitrile, pentane, or benzene, 5-aryl-2,2,4-trimethylfuran-3(2H)-ones (2), 6-aryl-6-hydroxy-3,3,5-trimethyl-1,2-dioxan-4-ones (3), and arene carboxylic acids (4) were produced via biradical-oxygen complexes, whereas in alcoholic solvents, 4-aryl-4-hydroxy-3,5,5-trimethyl-4,5-dihydrofuran-2(3H)-ones (5) were produced in addition to (2), (3), and (4).

Photochemical Reaction of 2,4-Dimethyl-1-phenylpentane-1,3-dione in the Presence of Oxygen. Formation of Furan-3(2H)-one and Peroxide

Yoshioka, Michikazu,Oka, Masashi,Ishikawa, Yuko,Tomita, Hideo,Hasegawa, Tadashi

, p. 639 - 640 (2007/10/02)

Photolysis of 2,4-dimethyl-1-phenylpentane-1,3-dione (1) in the presence of oxygen gave 2,2,4-trimethyl-5-phenylfuran-3(2H)-one (2) and 6-hydroxy-3,3,5-trimethyl-6-phenyl-1,2-dioxan-4-one (3) via the interaction of the type II biradical with oxygen.

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