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2,2,4,4-tetraphenyl-1,3-diselenacyclobutane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128632-60-0

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128632-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128632-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,6,3 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 128632-60:
(8*1)+(7*2)+(6*8)+(5*6)+(4*3)+(3*2)+(2*6)+(1*0)=130
130 % 10 = 0
So 128632-60-0 is a valid CAS Registry Number.

128632-60-0Relevant academic research and scientific papers

Isolation, Structure and Reaction of Selenobenzophenones. X-Ray Molecular Structure of 4,4'-Dimethoxyselenobenzophenone and of 4,4-Diphenyl-2,3-diselenabicyclooct-7-ene

Okuma, Kentaro,Kojima, Kazuki,Kaneko, Isao,Tsujimoto, Yoshikazu,Ohta, Hiroshi,Yokomori, Yoshinobu

, p. 2151 - 2160 (2007/10/02)

4,4'-Dimethoxy- 1a and 4,4'-dimethyl-selenobenzophenone 1b could be isolated in moderate yields by the reaction of the corresponding ylides 3 with elemental selenium in benzene at 80 deg C.Their spectral data are described.Attempted isolation of unsubstituted selenobenzophenone afforded only its dimer 5.Compound 1a crystallizes in space group P21/n with unit-cell parameters a = 7.191(3), b = 7.505(4=, c = 24.856(4) Angstroem, β = 90.32(1) deg, Z = 4, R = 0.055.The oxidation and thiation of 4,4'-dimethoxyselenobenzophenone 1a afforded the corresponding benzophenone and thiobenzophenone in good yields.The reaction of compound 1 with cyclopentadiene afforded the corresponding cycloadducts 7 (3,3-diaryl-2-selenabicyclohept-5-enes), whereas bicyclic diselenides 8 (4,4-diaryl-2,3-diselenabicyclooct-7-enes were obtained by using an excess of selenium and a higher temperature.Oxidation of compound 8c gave the corresponding diol 12, aldehyde 13, and diphenylfulvene 11.The reaction of compound 1a with benzenediazonium carboxylate afforded 2,2-bis-(4-methoxyphenyl)-4H-3,1-benzooxaselenin-4-one 17.

Isolation and Reaction of Selenobenzophenones

Okuma, Kentaro,Kojima, Kazuki,Kaneko, Isao,Ohta, Hiroshi

, p. 1053 - 1056 (2007/10/02)

4,4'-Dimethoxy- and 4,4'-dimethylselenobenzophenones could be isolated in moderate yields by the reaction of the corresponding ylides with selenium.Their spectral data are described.The oxidation of these compounds with mCPBA afforded the corresponding benzophenones in good yields.Attempted isolation of unsubstituted selenobenzophenone afforded only its dimer.

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