推荐产品
等级
p.a.
方案
99.0%
沸点
301 °C (lit.)
mp
47-50 °C (lit.)
密度
1.114 g/mL at 25 °C (lit.)
SMILES字符串
Nc1cccc2ccccc12
InChI
1S/C10H9N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7H,11H2
InChI key
RUFPHBVGCFYCNW-UHFFFAOYSA-N
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Danger
危险声明
危险分类
Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 1A
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
314.6 °F - closed cup
闪点(°C)
157 °C - closed cup
法规信息
新产品
Cüneyt Türkeş et al.
Journal of enzyme inhibition and medicinal chemistry, 30(4), 622-628 (2014-12-19)
In this study, we investigated the effects of antibacterial drugs (moxifloxacin hydrochloride, levofloxacin hemihidrate, cefepime hydrochloride, cefotaxime sodium and ceftizoxime sodium) on human serum paraoxonase-1 (hPON1) enzyme activity from human serum in vitro conditions. For this purpose, hPON1 enzyme was
Susanta Adhikari et al.
Dalton transactions (Cambridge, England : 2003), 44(32), 14388-14393 (2015-07-23)
The X-ray structurally characterized naphthalene appended diformyl-p-cresol derivative () selectively detects Sn(2+) by both colorimetric and fluorescence methods. In the presence of Sn(2+), exhibits a monomer emission at 420 nm along with a strong red excimer emission at 582 nm
F F Kadlubar et al.
Cancer research, 38(11 Pt 1), 3628-3638 (1978-11-01)
The carcinogen N-hydroxy-1-naphthylamine reacted with nucleic acids and protein under slightly acidic conditions (pH 5) to form covalently bound derivatives with 3 to 20 naphthyl residues/1000 monomer units. The level of binding was in the following order: DNA greater than
Andrew R Korte et al.
Analytical and bioanalytical chemistry, 407(8), 2301-2309 (2015-01-27)
A significant limiting factor in achieving high spatial resolution for matrix-assisted laser desorption ionization-mass spectrometry (MALDI-MS) imaging is the size of the laser spot at the sample surface. Here, we present modifications to the beam-delivery optics of a commercial MALDI-linear
Jayita Dutta et al.
Dalton transactions (Cambridge, England : 2003), 44(30), 13615-13632 (2015-07-07)
N-(Naphthyl)-4-R-salicylaldimines (R = OCH(3), H and Cl; H(2L)(1)-H(2)L(3)) and 2-hydroxy-N-(naphthyl)naphthaldimine (H(2)L(4)) readily undergo, upon reaction with Na(2)[PdCl(4)] in the presence of triphenylphosphine, cyclopalladation via C-H bond activation at the peri-position to afford complexes of type [Pd(L)(PPh(3))] (L = L(1)-L(4)). The
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