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4,5-dihydroacephenanthrylene is an organic compound with the molecular formula C16H12. It is a derivative of acenaphthylene, which is a polycyclic aromatic hydrocarbon consisting of two fused benzene rings and a cyclopentadiene ring. The "4,5-dihydro" prefix indicates that the compound has two additional hydrogen atoms, which are added across the double bond between the two benzene rings, making it a dihydro derivative. This modification can affect the compound's chemical properties, such as reactivity and stability, compared to the parent acenaphthylene. 4,5-dihydroacephenanthrylene is of interest in organic chemistry and materials science due to its potential applications in the synthesis of various compounds and its electronic properties.

6232-48-0

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6232-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6232-48-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,3 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6232-48:
(6*6)+(5*2)+(4*3)+(3*2)+(2*4)+(1*8)=80
80 % 10 = 0
So 6232-48-0 is a valid CAS Registry Number.

6232-48-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-dihydroacephenanthrylene

1.2 Other means of identification

Product number -
Other names Acephenanthrylene,4,5-dihydro

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:6232-48-0 SDS

6232-48-0Relevant 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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