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Aceanthrylene

Cholanthrene (l,2,-dihydrobenz[/]aceanthrylene) [479-23-2] M 254.3, m 173 . Crystd from benzene/diethyl ether. [Pg.169]

Synonym 20-methylcholanthrene, l,2-dihydro-3-methyl-benz[/]aceanthrylene... [Pg.821]

The numbering and lettering system for several PAHs is also given. Compounds are (1) naphthalene, (2) fluorene, (3) anthracene, (4) phenanthrene, (5) aceanthrylene, (6) benzo[a]-fluorene, (7) benzo[a]fluorene, (8) benzo[a]-fluorene, (9) fluoranthene, (10) naphthacene, (11) pyrene, (12) benzofluoranthene, (13) benzo[g,/r,fluoranthene, (14) perylene, (15) benzo[e]pyrene, (16) benzo[g,/),/]perylene, (17) anthanthrene, and (18) coronene. [Pg.1344]

Figure 2. Gas chromatogram of A, PAH fraction of diesel particulate extract (Sl-C2) and By its HPLC subfraction C (S1-C2). GC conditions 45- X 0.35-mm id SE54 glass capillary column flame ionization detector temperature, 110°C for 2 min, programmed to 170°C at 10°/min, to 212°C at 3°/min, to 278°C at 8°/min. Peak identities 1, phenanthrene 2, anthracene 3-6, methylanthracene/-phenan-threne 7, 2-phenylnaphthalene 8-10, dimethylanthracene/-phenanthrene 11, fluoranthene 12, aceanthrylene/acephenanthrylene 13, pyrene 14-15, trimethylan-thracene/-phenanthrene 16, benzo [ghi]fluoranthene 17, benzo[a/anthracene 18, triphenylene 19, chrysene 20, benzo[b]fluoranthene 21, benzo[]]fluoranthene ... Figure 2. Gas chromatogram of A, PAH fraction of diesel particulate extract (Sl-C2) and By its HPLC subfraction C (S1-C2). GC conditions 45- X 0.35-mm id SE54 glass capillary column flame ionization detector temperature, 110°C for 2 min, programmed to 170°C at 10°/min, to 212°C at 3°/min, to 278°C at 8°/min. Peak identities 1, phenanthrene 2, anthracene 3-6, methylanthracene/-phenan-threne 7, 2-phenylnaphthalene 8-10, dimethylanthracene/-phenanthrene 11, fluoranthene 12, aceanthrylene/acephenanthrylene 13, pyrene 14-15, trimethylan-thracene/-phenanthrene 16, benzo [ghi]fluoranthene 17, benzo[a/anthracene 18, triphenylene 19, chrysene 20, benzo[b]fluoranthene 21, benzo[]]fluoranthene ...
Scott, L. T. Roelofs, N. H. 1987 Benzene ring contractions at high temperatures. Evidence from the thermal interconversions of aceanthrylene, acephenanthrylene and fluoranthrene. J. Am. chem. Soc. 109, 5461-5465. [Pg.16]

Likewise, the alkynyl 3-(2-iodophenyl) indole 191 is transformed under similar conditions into the 6,7-dihydro-5H-4b-aza-benzo[a]aceanthrylene 192 in good yield (Scheme 74). [Pg.190]

DIHYDRO-4-METHOXY-l-METH L-2-OXONTCOTINONITRILE see RJKIOO S-(2,3-DIHYDRO-5-METHOXY-2-OXO-l,3,4-THIADIAZOL-3-METHYL) see DSOOOO 10.11-DIHYDRO-5-(3-(METHYLAi nNO)PROPYL)-5H-DIBENZ(b,f)AZEPINE HYDROCHLORIDE see DLS600 1. a-DinYDRO-O-METHTT--BENZ(j)ACEANTHRYLENE see nj750... [Pg.1632]

C23H27N05 fmoc-O-t-butyl-L-threonine 71989-35-0 25.00 1.1670 2 33726 C24H14 dibenz(a,j)aceanthrylene 203-20-3 25.00 1.1762 2... [Pg.287]

C19H38 2-methyl-1-octadecene 61868-20-0 602.15 53.780 1,2 31835 C20H12O 9,10-epoxy-9,10-dihydrobenz(j)aceanthrylene 1X933-92-5 520.65 45.872 1.2... [Pg.538]

A mixture of four dimers (8X) is obtained from the benzophenone-sensitized irradiation of the triene (164). Vacuum sublimation of this mixture affords the dimer (165) which was subsequently converted by conventional chemical paths to the hydrocarbon (166).Photosensitized (Rose Bengal) dimerization of aceanthrylene (167) has been studied in methanol solution. This affords both the syn- and anti-head-to-head and head-to-tail stereoisomers. The results indicate that there is a slight preference for the formation of the syn-adduc t s. ... [Pg.273]

The higher homologs of acenaphthylene dianion 82 are the aceanthrylene dianion 33 and acephenanthrylene dianion 34 122,123). The convenient synthesis of the the hydrocarbon enabled a detailed investigation of their metal reduction and the exploration of their patterns of delocalization. Despite their being (4n + 2)ji-electron systems, these anions are not diatropic as one may expect from counting their jc-electrons. [Pg.129]

Mass MJ. Jeffers AJ, Ross JA, et al. Ki-ras oncogene mutations in tumors and DNA adducts formed by benz[j]aceanthrylene and benzo[a]pyrene in the lungs of strain A/J mice. Mol Carcinogen 8 186-192. [Pg.490]

Hegstad, S., Lundanes, E., Holme, J. A., and Alexander, J. (1999). Characterization of metabolites of benz(/)aceanthrylene in faeces, urine and bile from rat. Xenobiotica 29, 1257-1272. [Pg.187]


See other pages where Aceanthrylene is mentioned: [Pg.19]    [Pg.348]    [Pg.405]    [Pg.469]    [Pg.166]    [Pg.19]    [Pg.254]    [Pg.482]    [Pg.482]    [Pg.77]    [Pg.87]    [Pg.439]    [Pg.1614]    [Pg.482]    [Pg.19]    [Pg.282]    [Pg.282]    [Pg.284]    [Pg.286]    [Pg.287]    [Pg.538]    [Pg.538]    [Pg.538]    [Pg.539]    [Pg.218]    [Pg.346]    [Pg.181]   
See also in sourсe #XX -- [ Pg.77 , Pg.87 ]

See also in sourсe #XX -- [ Pg.155 , Pg.156 ]

See also in sourсe #XX -- [ Pg.648 ]

See also in sourсe #XX -- [ Pg.253 ]




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