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5-Methoxy-7-methylbenz[a]anthracene is a polycyclic aromatic hydrocarbon (PAH) with the chemical formula C19H16O. It is a derivative of benz[a]anthracene, featuring a methyl group at the 7th position and a methoxy group at the 5th position. 5-Methoxy-7-methylbenz[a]anthracene is known for its potential mutagenicity and carcinogenicity, as it can interact with DNA and cause mutations, which may lead to cancer. It is also a significant environmental pollutant, often found in tobacco smoke, coal tar, and other combustion products. Due to its hazardous properties, research on 5-methoxy-7-methylbenz[a]anthracene focuses on understanding its mechanisms of action and developing methods for its detection and mitigation in the environment and human exposure.

966-48-3

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966-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 966-48-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 966-48:
(5*9)+(4*6)+(3*6)+(2*4)+(1*8)=103
103 % 10 = 3
So 966-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H16O/c1-13-15-8-4-3-7-14(15)11-19-16-9-5-6-10-17(16)20(21-2)12-18(13)19/h3-12H,1-2H3

966-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxy-7-methylbenzo[a]anthracene

1.2 Other means of identification

Product number -
Other names 5-methoxy-7-methyltetraphene

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:966-48-3 SDS

966-48-3Relevant academic research and scientific papers

Sterically Induced Methoxyl Migration on Acid-Catalyzed Dehydration of K-Region trans-Dihydrodiol Monomethyl Ethers

Nashed, Nashaat T.,Rao, Tata Venkata S.,Jerina, Donald M.

, p. 6344 - 6348 (2007/10/02)

The regioisomers of the trans-dihydrodiol monomethyl esters (DME) at the K-regions of 4- and 7-methyl- and 7,12-dimethylbenzanthracene, which possess a ring methyl substituent peri to the methoxyl group, react with BF3*etherate to form a single phenol and two regioisomeric phenol methyl ethers, one of which arises by migration of the methoxyl group.In contrast, for DME of benzanthracene and its 1-, 4-, 7-, 11- and 12-methyl- and 7,12-dimethyl-substituted derivatives where there is no peri methyl group, methoxyl migration does not occur, and thus only the phenol methyl ether resulting from loss of water is formed.These results are consistent with a mechanism in which the initially formed carbocation with a pseudoaxial methoxy group must undergo either conformational change to align the bond of the leaving proton with the empty p-orbital prior to proton loss or migration of the methoxyl group to the adjacent carbocation via a cyclic oxonium ion.In the absence of a ring substituent peri to the methoxyl group, conformational change is faster than formation of the cyclic oxonium ion, and therefore migration of the methoxyl group does not occur.A methyl substituent peri to the methoxyl group raises the activation energy barrier for conformational isomerization due to adverse steric interaction between the two groups.Consequently, formation of the cyclic oxonium ion becomes competitive with conformational change.The resulting oxonium ion opens to the regioisomeric carbocation resulting in rearrangement.Formation of the cyclic oxonium ion in these reactions is analogous to the rapid internal return of the hydroxy carbocation intermediate to protonated epoxide that is thought to occur in the reactions of peri-methyl-substituted K-region arene oxides.

Solvolysis of K-region arene oxides: Substituent effects on reactions of benz[a]anthracene 5,6-oxide

Nashed, Nashaat T.,Balani, Suresh K.,Loncharich, Richard J.,Sayer, Jane M.,Shipley, David Y.,Mohan, Ram S.,Whalen, Dale L.,Jerina, Donald M.

, p. 3910 - 3919 (2007/10/02)

The solvolytic reactivity and products formed from benz[a]anthracene 5,6-oxide (BA-O) on substitution of a methyl group at positions 1 (1-MBA-O), 4 (4-MBA-O), 7 (7-MBA-O), 11 (11-MBA-O), and 12 (12-MBA-O), on 7,12-dimethyl substitution (7,12-DMBA-O), and on 7-bromo substitution in 1:9 dioxane-water and in methanol at 25°C are reported. These substitutions result in > 150-fold differences in their rates of acid-catalyzed solvolysis and cause marked changes in the distribution of solvent adducts and phenols resulting from isomerization. Optically pure BA-O, 7-MBA-O, 12-MBA-O, and 7,12-DMBA-O as well as their optically pure trans dihydrodiols were utilized to determine the point of attack by water in the hydrolysis reactions. In general, the reactions in aqueous dioxane (0.1 M NaClO4) obeyed the rate equation kobsd = kH[H+] + k0, where kH is the second-order rate constant for acid-catalyzed reaction and k0 is the first-order rate constant for spontaneous reaction, to provide biphasic pH-rate profiles. When ionic strength was maintained with 0.5 M KCl, however, more complex pH-rate profiles were observed for some of the arene oxides due to attack of chloride on the neutral epoxide to produce steady-state concentrations of chlorohydrins. Rate enhancement on methyl substitution is largest (kH, ca. 5-fold) when the methyl group is present in the hindered bay region (C1 or C12) or adjacent to the epoxide at C7. The combined effect of two methyl groups (7,12-DMBA-O) is additive (ca. 25-fold). Theoretical calculations (molecular mechanics by PCMODEL-PI and ab initio by GAUSSIAN 86 and 88 programs) of carbocation stability indicate the importance of steric factors in determining relative reactivity and types of products formed from substituted benz[a]anthracene 5,6-oxides.

Oxygen Sensitization of Electron Capture Response to Isomers of Polycyclic Aromatic Amines and Hydroxides

Campbell, J. A.,Grimsrud, E. P.,Hageman, L. R.

, p. 1335 - 1340 (2007/10/02)

The use of the oxygen-sensitized constant-current electron capture detector (ECD) with gas chromatography for analyte identification is extended by examining the responses of numerous polycyclic aromatic amines and hydroxides where an appropriate EC-enhancing chemical tag has been attached to the amino group or the hydroxy group has been methylated.For the majority of isomeric groups examined, measured response enhancements of the derivatives are sufficiently dependent on structural differences as to provide an additional means by which substitution isomers can be differentiated.The ion chemistry responsible for the EC and oxygen-sensitized responses also has been examined by the use of an atmospheric pressure ionization mass spectrometer (APIMS).

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