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(4-Methoxybenzyl)(4-nitrophenyl)selane is an organoselenium compound characterized by a selenium atom bonded to a 4-methoxybenzyl group and a 4-nitrophenyl group. This molecule is a type of selenide, which is a derivative of selenium analogous to the sulfides found in organic chemistry. The 4-methoxybenzyl group contributes a methoxy (-OCH3) functional group attached to a benzene ring, while the 4-nitrophenyl group features a nitro (-NO2) functional group on a benzene ring. The combination of these functional groups gives the compound unique chemical properties, such as reactivity and stability, making it potentially useful in various chemical reactions and applications, including synthetic organic chemistry and materials science.

97338-68-6

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97338-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97338-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,3 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97338-68:
(7*9)+(6*7)+(5*3)+(4*3)+(3*8)+(2*6)+(1*8)=176
176 % 10 = 6
So 97338-68-6 is a valid CAS Registry Number.

97338-68-6Downstream Products

97338-68-6Relevant academic research and scientific papers

Diselenide-Mediated Catalytic Functionalization of Hydrophosphoryl Compounds

Handoko,Benslimane, Zacharia,Arora, Paramjit S.

supporting information, p. 5811 - 5816 (2020/07/27)

We report a diaryldiselenide catalyst for cross-dehydrogenative nucleophilic functionalization of hydrophosphoryl compounds. The proposed organocatalytic cycle closely resembles the mechanism of the Atherton-Todd reaction, with the catalyst serving as a recyclable analogue of the halogenating agent employed in the named reaction. Phosphorus and selenium NMR studies reveal the existence of a P-Se bond intermediate, and structural analyses indicate a stereospecific reaction.

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