P11603
9-Phenanthrenecarboxaldehyde
97%
동의어(들):
9-Formylphenanthrene, 9-Phenanthraldehyde, 9-Phenanthrenaldehyde, 9-Phenanthrenecarbaldehyde, 9-Phenanthridinecarboxaldehyde, Phenanthrene-9-carboxaldehyde
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모든 사진(1)
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2.5 G
₩145,348
10 G
₩552,262
About This Item
실험식(Hill 표기법):
C15H10O
CAS Number:
Molecular Weight:
206.24
Beilstein:
511309
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
97%
양식
powder
mp
100-103 °C (lit.)
SMILES string
[H]C(=O)c1cc2ccccc2c3ccccc13
InChI
1S/C15H10O/c16-10-12-9-11-5-1-2-6-13(11)15-8-4-3-7-14(12)15/h1-10H
InChI key
QECIGCMPORCORE-UHFFFAOYSA-N
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
이미 열람한 고객
Danuta Sek et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 175, 24-35 (2016-12-25)
The new Schiff bases bearing anthracene unit were synthesized from 2-aminoanthracene and various aldehydes such as: benzaldehyde, 4-(diphenylamino)benzaldehyde, 9-phenanthrenecarboxaldehyde, 9-anthracenecarboxaldehyde, and biphenyl-4-carboxaldehyde, 2-naphthaldehyde. Resulted azomethines were characterized by IR, NMR (
Chiara Giorio et al.
Chemosphere, 224, 786-795 (2019-03-10)
Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous atmospheric pollutants of high concern for public health. In the atmosphere they undergo oxidation, mainly through reactions with ·OH and NOx to produce nitro- and oxygenated (oxy-) derivatives. In this study, we developed a
Paulo Cicero Nascimento et al.
Journal of separation science, 38(23), 4055-4062 (2015-10-09)
Liquid chromatography coupled to mass spectrometry with atmospheric pressure chemical ionization was used for the determination of polycyclic aromatic hydrocarbon derivatives, the oxygenated polycyclic aromatic hydrocarbons and nitrated polycyclic aromatic hydrocarbons, formed in asphalt fractions. Two different methods have been
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