InChI
1S/C9H7N/c1-2-4-9-7-10-6-5-8(9)3-1/h1-7H
InChI key
AWJUIBRHMBBTKR-UHFFFAOYSA-N
SMILES string
c1ccc2cnccc2c1
grade
purum
assay
≥97.0% (GC)
refractive index
n20/D 1.623 (lit.)
bp
242-243 °C (lit.)
mp
26-28 °C (lit.)
density
1.099 g/mL at 25 °C (lit.)
storage temp.
2-8°C
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
215.6 °F - closed cup
flash_point_c
102 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
新产品
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Jörg T Binder et al.
Journal of the American Chemical Society, 134(41), 17003-17006 (2012-10-09)
We have developed a nickel-catalyzed method for the asymmetric cross-coupling of secondary electrophiles with secondary nucleophiles, specifically, stereoconvergent Negishi reactions of racemic benzylic bromides with achiral cycloalkylzinc reagents. In contrast to most previous studies of enantioselective Negishi cross-couplings, tridentate pybox
Qiuhong Zhou et al.
Talanta, 99, 932-938 (2012-09-13)
A simple and rapid method based on microwave-assisted extraction (MAE) followed by capillary electrophoresis (CE) was developed for the quantification of eight isoquinoline alkaloids in Chelidonium majus L. (Ch. majus). The key parameters affecting CE separation and MAE extraction were
Xuan Xing et al.
Chemosphere, 86(4), 368-375 (2011-11-11)
Nitrogen-heterocyclic compounds (NHCs) are toxic and bio-refractory contaminants widely spread in environment. This study investigated electrochemical degradation of NHCs at boron-doped diamond (BDD) anode with particular attention to the effect of different number and position of nitrogen atoms in molecular
Giordano Mancini et al.
PloS one, 7(12), e51354-e51354 (2012-12-14)
Long-duration comparative molecular dynamics simulations of the DNA-topoisomerase binary and DNA-topoisomerase-indenoisoquinoline ternary complexes have been carried out. The analyses demonstrated the role of the drug in conformationally stabilizing the protein-DNA interaction. In detail, the protein lips, clamping the DNA substrate
Abdol R Hajipour et al.
Bioorganic & medicinal chemistry, 19(24), 7435-7440 (2011-11-08)
The sigma-2 (σ2) receptor has been suggested to be a promising target for pharmacological interventions to curb tumor progression. Development of σ2-specific ligands, however, has been hindered by lack of understanding of molecular determinants that underlie selective ligand-σ2 interactions. Here
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