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1,2,4,5-Tetrabenzoylbenzene is an organic compound with the molecular formula C30H18O4. It is a derivative of benzene, where four benzoyl groups (C6H5CO) are attached to the benzene ring at positions 1, 2, 4, and 5. 1,2,4,5-tetrabenzoylbenzene is characterized by its symmetrical structure and is often used as a precursor in the synthesis of various organic compounds, such as dyes and pharmaceuticals. Due to its aromatic nature and the presence of multiple benzoyl groups, 1,2,4,5-tetrabenzoylbenzene exhibits unique chemical properties, including stability and reactivity towards certain chemical reactions. It is typically synthesized through the Friedel-Crafts acylation reaction, where benzoyl chloride reacts with benzene in the presence of a Lewis acid catalyst. The compound's applications span across various fields, including materials science, pharmaceuticals, and chemical research, making it a significant molecule in the realm of organic chemistry.

3867-56-9

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3867-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3867-56-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,6 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3867-56:
(6*3)+(5*8)+(4*6)+(3*7)+(2*5)+(1*6)=119
119 % 10 = 9
So 3867-56-9 is a valid CAS Registry Number.

3867-56-9Relevant academic research and scientific papers

Solvent effects in the reaction between (anthracen-9-yl)methyl sulfides and electron-deficient acetylenes

Gopalakrishnan, Reshma,Jacob, Jomon P.,Mallia, Rekha R.,Unnikrishnan, Perupparampil A.,Prathapan, Sreedharan

, p. 472 - 479 (2015/06/30)

Solvent-dependent diverse reactivity of (anthracen-9-yl)methyl sulfides with a few electron-deficient acetylenes is described. Diversity in reactivity is attributed to competition between one electron transfer, two electron transfer and Diels-Alder reaction of these sulfides with electron-deficient acetylenes. We have proposed plausible mechanisms to account for various reactions observed by us.

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