About This Item
Fórmula linear:
C10H6(CH3)2
Número CAS:
Peso molecular:
156.22
Beilstein:
1852737
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
99%
Formulário
solid
p.e.
263 °C (lit.)
pf
94-97 °C (lit.)
cadeia de caracteres SMILES
Cc1ccc2ccc(C)cc2c1
InChI
1S/C12H12/c1-9-3-5-11-6-4-10(2)8-12(11)7-9/h3-8H,1-2H3
chave InChI
LRQYSMQNJLZKPS-UHFFFAOYSA-N
Informações sobre genes
human ... CYP1A2(1544)
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Categorias relacionadas
Descrição geral
The atmospheric oxidation mechanism of 2,7-dimethylnaphthalene initiated by OH radical was investigated. Adsorption of 2,7-dimethylnaphthalene isomers dissolved in supercritical carbon dioxide on NaY-type zeolite was also studied.
Aplicação
2,7-Dimethylnaphthalene was used in the preparation of 2,7-bisbromomethylnapthalene via bromination with N-bromosuccinimide.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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243. Eight-and higher-membered ring compounds. Part V. Di-(naphthalene-2: 7-dimethylene) and its conversion into coronene.
Baker W, et al.
Journal of the Chemical Society, 1118-1121 (1951)
Adsorption of supercritical carbon dioxide+ 2, 6-and 2, 7-dimethylnaphthalene isomers on NaY-type zeolite.
Iwai Y, et al.
Industrial & Engineering Chemistry Research, 42(21), 5261-5267 (2003)
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The journal of physical chemistry. A, 117(1), 160-168 (2012-12-12)
The atmospheric oxidation mechanism of 2,7-dimethylnaphthalene (27DMN) initiated by OH radical is investigated at levels of BB1K and G3MP2-RAD//BH&HLYP. The reaction is mainly initiated by OH addition to the C(1) position to form radical adduct R1. In the atmosphere, R1
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Three fishing harbors were investigated to study the polycyclic aromatic hydrocarbons in the sediments and trace possible anthropogenic sources by identification of cyclic terpenoid biomarkers. Seventeen terpanes, 10 steranes and 10 bicyclic sesquiterpanes in the marine diesel and the three
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A series of naphthalene and non-naphthalene derivatives (n=42) having cytochrome P450 2A6 and 2A5 inhibitory activities, reported by Rahnasto et al., were subjected to QSAR and QAAR studies. The analyses were performed using electronic, spatial, shape and thermodynamic descriptors to
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