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4,5,7,8,9,10-Hexahydroacephenanthrylene is a polycyclic aromatic hydrocarbon (PAH) with a molecular formula of C16H14. It is a derivative of acenaphthylene, which is a structural isomer of naphthalene. 4,5,7,8,9,10-hexahydroacephenanthrylene consists of a hexagonal ring fused to a five-membered ring, with six hydrogen atoms attached to the carbon atoms in the hexagonal ring. 4,5,7,8,9,10-Hexahydroacephenanthrylene is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its complex structure and potential applications, it has been the subject of research in organic chemistry and material science. However, like other PAHs, it may also exhibit toxic properties and require proper handling and disposal.

7468-93-1

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7468-93-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7468-93-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7468-93:
(6*7)+(5*4)+(4*6)+(3*8)+(2*9)+(1*3)=131
131 % 10 = 1
So 7468-93-1 is a valid CAS Registry Number.

7468-93-1Downstream Products

7468-93-1Relevant academic research and scientific papers

Synthesis and spectroscopy of nine isomeric methylacephenanthrylenes

Mulder, Patrick P. J.,Boere, Ben B.,Baart, Arthur,Cornelisse, Jan,Lugtenburg, Johan

, p. 22 - 32 (2007/10/02)

The synthesis of nine isomeric methyl-substituted acephenanthrylenes is described.Three different approaches were used. 1-, 2-, And 6-methylacephenanthrylene (1a, 1c and 1f) were prepared by formylation of acephenanthrene (2) and 4,5,7,8,9,10-hexahydroacephenanthrylene (17), followed by Wolff-Kishner reduction and dehydrogenation. 4-, 5-, 7- And 10-methylacephenanthrylene (1d, 1e, 1g and 1j) were synthesized by treating the corresponding acephenanthrenones with methyllithium, followed by dehydration and, in the case of 1g and 1j, dehydrogenation. 8- And 9-methylacephenanthrylene (1h and 1i) were prepared by a Haworth synthesis starting with the reaction of methylsuccinic anhydride with acenaphthene. the spectroscopic properties of acephenanthrylene and its methyl derivatives were investigated with mass spectrometry, (1)H NMR and UV-VIS spectroscopy.According to the (1)H NMR spectra, steric hindrance between the methyl group and nearby protons decreases in the following order: 1, 10 > 6 > 7 > 3 > 4, 5, 8, 9.

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