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Merck
CN

360740

Sigma-Aldrich

1,2-二甲基萘

95%

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线性分子式:
C10H6(CH3)2
CAS号:
分子量:
156.22
Beilstein:
2039376
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

95%

折射率

n20/D 1.615 (lit.)

bp

266-267 °C (lit.)

mp

−2-−1 °C (lit.)

密度

1.013 g/mL at 25 °C (lit.)

SMILES字符串

Cc1ccc2ccccc2c1C

InChI

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

InChI key

QNLZIZAQLLYXTC-UHFFFAOYSA-N

基因信息

human ... CYP1A2(1544)

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一般描述

1,2-Dimethylnaphthalene is a polycyclic aromatic hydrocarbon. Its effect on the naupliar and adult stages of the marine cyclopoid copepod Oithona davisae is reported.

应用

1,2-Dimethylnaphthalene is suitable reagent used to investigate the secondary organic aerosol (SOA) production via gas-phase photooxidation.

WGK

WGK 3

闪点(°F)

235.4 °F

闪点(°C)

113 °C

个人防护装备

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


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Secondary organic aerosol formation from photooxidation of naphthalene and alkylnaphthalenes: implications for oxidation of intermediate volatility organic compounds (IVOCs).
Chan AWH, et al.
Atmospheric Chemistry and Physics, 9(9), 3049-3060 (2009)
A Kilanowicz et al.
International journal of occupational medicine and environmental health, 11(4), 305-317 (1999-02-24)
The aim of this study was to investigate the distribution, excretion and metabolism of 1,2-dimethylnaphthalene-[ring-U-3H] in rats. The experiments were performed on 54 male outbred IMP:Wist rats with body weight of 200 g +/- 20%. The compound was given i.p.
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
Laura E Korhonen et al.
Journal of medicinal chemistry, 48(11), 3808-3815 (2005-05-27)
The purpose of this study was to determine the cytochrome P450 1A2 (CYP1A2) inhibition potencies of structurally diverse compounds to create a comprehensive three-dimensional quantitative structure-activity relationship (3D-QSAR) model of CYP1A2 inhibitors and to use this model to predict the
Minna Rahnasto et al.
Journal of medicinal chemistry, 48(2), 440-449 (2005-01-22)
The purpose of this study was to develop screening and in silico modeling methods to obtain accurate information on the active center of CYP2A6, a nicotine oxidizing enzyme. The inhibitory potencies of 26 naphthalene and 16 non-naphthalene derivatives were determined

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