方案
98%
mp
274-278 °C (lit.)
SMILES字符串
c1ccc(cc1)-c2nc(-c3ccccc3)c([nH]2)-c4ccccc4
InChI
1S/C21H16N2/c1-4-10-16(11-5-1)19-20(17-12-6-2-7-13-17)23-21(22-19)18-14-8-3-9-15-18/h1-15H,(H,22,23)
InChI key
RNIPJYFZGXJSDD-UHFFFAOYSA-N
基因信息
rat ... Soat1(81782)
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储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
K Nakashima et al.
Biomedical chromatography : BMC, 11(2), 63-64 (1997-03-01)
A rapid and convenient flow-injection method is described for the determination of Co(II). The method utilized the phenomenon that the lophine-Co(II)-H2O2 chemiluminescence (CL) reaction is enhanced in alkaline media by the addition of hydroxylammonium chloride. The calibration curve was linear
Yong Sheng Zhao et al.
Physical chemistry chemical physics : PCCP, 8(28), 3300-3303 (2006-07-13)
Nanocrystals with tunable morphologies and optical properties were successfully fabricated from an organic functional low-molecular-weight compound, 2,4,5-triphenylimidazole (lophine), through a sonication technique.
Yong Sheng Zhao et al.
Journal of nanoscience and nanotechnology, 7(3), 1021-1027 (2007-04-25)
Copper/lophine core/shell nanocomposites were fabricated through the self-assembly of lophine on the surfaces of copper nanostructures. The growth of the lophine shells was induced by the cooperation of coordination and several other noncovalent interactions. The dimensions, structures, and morphologies of
M Kimura et al.
Luminescence : the journal of biological and chemical luminescence, 22(2), 72-76 (2006-11-08)
Singlet oxygen was detected from the reaction of lophine hydroperoxides 2 in the presence of 1,3-diphenyl-isobenzofuran as a singlet oxygen detector. In order to examine the substituent effect on the formation of (1)O(2), 2-(p-substituted phenyl) lophine peroxides 2a-c were tested.
Kenichiro Nakashima
Biomedical chromatography : BMC, 17(2-3), 83-95 (2003-04-30)
Lophine (2,4,5-triphenylimidazole) derivatives as versatile analytical tools in biomedical sciences are described. Chemiluminescence (CL) and fluorescence (FL) properties of the lophine derivatives are first demonstrated including the CL reaction mechanism, effects of substituents on CL yields, FL spectral behaviors, etc.
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