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279919

Sigma-Aldrich

2,7-Dimethylnaphthalene

99%

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About This Item

Formula condensata:
C10H6(CH3)2
Numero CAS:
582-16-1
Peso molecolare:
156.22
Beilstein:
1852737
Numero CE:
209-477-1
Numero MDL:
MFCD00004121
Codice UNSPSC:
12352100
ID PubChem:
24856917
NACRES:
NA.22

Saggio

99%

Stato

solid

P. ebollizione

263 °C (lit.)

Punto di fusione

94-97 °C (lit.)

Stringa SMILE

Cc1ccc2ccc(C)cc2c1

InChI

1S/C12H12/c1-9-3-5-11-6-4-10(2)8-12(11)7-9/h3-8H,1-2H3
LRQYSMQNJLZKPS-UHFFFAOYSA-N

Informazioni sul gene

human ... CYP1A2(1544)

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Categorie correlate

Descrizione generale

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.

Applicazioni

2,7-Dimethylnaphthalene was used in the preparation of 2,7-bisbromomethylnapthalene via bromination with N-bromosuccinimide.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
SHBD2967V
08896PMV
08896PM
10710JE
04505MV

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Sigma-Aldrich

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Sigma-Aldrich

764094

1,8-Dibromonaphthalene

2,6-Bis(bromomethyl)naphthalene 95%

Sigma-Aldrich

649546

2,6-Bis(bromomethyl)naphthalene

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)
Zhijie Zhang et al.
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
Nien-Hsin Kao et al.
Marine pollution bulletin, 97(1-2), 319-332 (2015-06-08)
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
Kunal Roy et al.
European journal of medicinal chemistry, 44(5), 1941-1951 (2008-12-27)
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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