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279919

Sigma-Aldrich

2,7-Dimethylnaphthalene

99%

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About This Item

Linear Formula:
C10H6(CH3)2
CAS Number:
582-16-1
Molecular Weight:
156.22
Beilstein/REAXYS Number:
1852737
EC Number:
209-477-1
MDL number:
MFCD00004121
UNSPSC Code:
12352100
PubChem Substance ID:
24856917
NACRES:
NA.22

assay

99%

form

solid

bp

263 °C (lit.)

mp

94-97 °C (lit.)

SMILES string

Cc1ccc2ccc(C)cc2c1

InChI

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

InChI key

LRQYSMQNJLZKPS-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544)

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General description

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.

Application

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000253686
0000253682
0000216816
0000242992
SHBD2967V

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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
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)
Xu-Hui Huang et al.
Food & function, 12(4), 1626-1638 (2021-01-22)
Clam is a kind of nutritious, delicious and economical aquatic food around the world and is famous for its unique aroma. Instrumental analysis, sensory analysis, and comprehensive statistical analysis were performed to explain the relationship between aroma and odorants in
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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