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3,6-Bis-(4-fluoro-phenyl)-[1,2,4,5]tetroxane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75895-51-1

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75895-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75895-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,9 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75895-51:
(7*7)+(6*5)+(5*8)+(4*9)+(3*5)+(2*5)+(1*1)=181
181 % 10 = 1
So 75895-51-1 is a valid CAS Registry Number.

75895-51-1Downstream Products

75895-51-1Relevant academic research and scientific papers

Iodine-catalyzed one-pot synthesis and antimalarial activity evaluation of symmetrically and asymmetrically substituted 3,6-diphenyl[1,2,4,5]tetraoxanes

Kumar, Nitin,Khan, Shabana I.,Sharma, Mukul,Atheaya, Himanshu,Rawat, Diwan S.

scheme or table, p. 1675 - 1677 (2009/10/15)

A novel iodine-catalyzed one-pot synthesis of symmetrically and asymmetrically substituted 3,6-diphenyl-[1,2,4,5]tetraoxanes is described. The synthetic protocol is general with substituted benzaldehydes and proceeds well under acidic conditions. Total 17

Synthesis, thermal stability, antimalarial activity of symmetrically and asymmetrically substituted tetraoxanes

Atheaya, Himanshu,Khan, Shabana I.,Mamgain, Ritu,Rawat, Diwan S.

, p. 1446 - 1449 (2008/12/21)

Symmetrically and asymmetrically substituted 1,2,4,5-tetraoxanes were synthesized by the oxidative system H2O2/TFE in presence of MeReO3 as a catalyst. All of the synthesized compounds were characterized spectroscopically,

Synthesis and antimalarial activity of cyclic peroxides, 1,2,4,5,7- pentoxocanes and 1,2,4,5-tetroxanes

Kim, Hye-Sook,Shibata, Yasuharu,Wataya, Yusuke,Tsuchiya, Kaoru,Masuyama, Araki,Nojima, Masatomo

, p. 2604 - 2609 (2007/10/03)

A variety of 1,2,4,5,7-pentoxocane and 1,2,4,5-tetroxane derivatives were prepared as potential peroxide antimalarial agents. In both series of cyclic peroxides, the steric and electronic effects of the substituents attached to the peroxide ring exert a r

FUNCTIONAL ORGANIC PEROXIDES XIV. EFFECT OF FLUORINE ATOMS AND FLUORINE-CONTAINING SUBSTITUENTS IN BENZALDEHYDE ON THE DIRECTION OF THE REACTION WITH HYDROGEN PEROXIDE

Rakhimov, A. I.,Chapurkin, V. V.,Yagupol'skii, L. M.,Kondratenko, N. V.

, p. 1272 - 1275 (2007/10/02)

The reaction of m- and p-fluoro-, pentafluoro-, m-, and p-trifluoromethyl-, and o- and p-difluoromethoxybenzaldehydes with hydrogen peroxide was investigated.It was established that the initial reaction products are the corresponding α-hydroxy hydroperoxi

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