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1,5-diselenacyclooctane is a cyclic organoselenium compound with the molecular formula C8H14Se2. It consists of an eight-membered carbon ring with two selenium atoms incorporated at the 1st and 5th positions, forming a unique structure. 1,5-diselenacyclooctane is of interest in the field of organoselenium chemistry due to its potential applications in various chemical reactions and as a precursor for the synthesis of other selenium-containing compounds. The presence of selenium atoms in the molecule can impart unique properties, such as enhanced reactivity or stability, making 1,5-diselenacyclooctane a valuable building block in the development of new materials and pharmaceuticals.

6572-97-0

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6572-97-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6572-97-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6572-97:
(6*6)+(5*5)+(4*7)+(3*2)+(2*9)+(1*7)=120
120 % 10 = 0
So 6572-97-0 is a valid CAS Registry Number.

6572-97-0Downstream Products

6572-97-0Relevant academic research and scientific papers

?-BONDED DICATIONS FROM MEDIUM-SIZED SELENIUM AND TELLURIUM HETEROCYCLES

Fujihara, Hisashi,Furukawa, Naomichi

, p. 131 - 134 (2007/10/02)

The two-electron oxidation of 1,5-diselenacyclooctane (1) or 1,5-ditelluracyclooctane (3) with 2 equiv of NOBF4 gave the diselenide dication salt, 1,5-diselenoniabicyclooctane bis(tetrafluoroborate) (2), or the ditelluride dication salt 4.The structures of the dications were characterized by 77Se and 125Te NMR spectroscopy and X-ray crystallographic analysis.The diselenide dication salt 6 having aromatic ring was formed in the reaction of 5H,7H-dibenzodiselenocin 6-oxide (5) with 2 equiv of silylating reagent, CF3SO3SiMe3.These dications react either as an oxidant or as an electrophile depending on the added reagent.

Reactivity of Diselenide Dication Salt, 1,5-Diselenoniabicyclooctane Bis(hexafluorophosphate) toward Aromatics. A New Mode of Aromatic Substitution and Redox Reaction

Fujihara, Hisashi,Nakamura, Akiko,Akaishi, Ryouichi,Furukawa, Naomichi

, p. 393 - 396 (2007/10/02)

A new diselenide dication salt, 1,5-diselenoniabicyclooctane bis(hexafluorophosphate) was reacted with several aromatics to afford either the substitution or redox products.The reaction mode depends on the oxidation potential of aromatics.

CHEMICAL AND ELECTROCHEMICAL REDUCTION OF DISELENIDE DICATION SALT, 1,5-DISELENONIABICYCLOOCTANE BIS(HEXAFLUOROPHOSPHATE)

Fujihara, Hisashi,Akaishi, Ryouichi,Nakamura, Akiko,Furukawa, Naomichi

, p. 6375 - 6378 (2007/10/02)

The reaction of the diselenide dication salt, 1,5-diselenoniabicyclooctane bis(hexafluorophosphate) (1) with 1,5-diselenacyclooctane (2) gave the corresponding cation radical by single-electron transfer.The dication salt 1 was reduced upon treatment with fluorenyl-lithium, Na2S, NaBH4; it did not deprotonate.The cyclic voltammetry of 1 shows the reversible reduction peak at remarkably low reduction potential.

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