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P11603

9-Phenanthrenecarboxaldehyde

Name: 9-Phenanthrenecarboxaldehyde
Brand: ALDRICH

97%

Synonym(s):

9-Formylphenanthrene, 9-Phenanthraldehyde, 9-Phenanthrenaldehyde, 9-Phenanthrenecarbaldehyde, 9-Phenanthridinecarboxaldehyde, Phenanthrene-9-carboxaldehyde

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About This Item

Empirical Formula (Hill Notation):

C₁₅H₁₀O

CAS Number:

4707-71-5

Molecular Weight:

206.24

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24898165

EC Number:

225-194-6

Beilstein/REAXYS Number:

511309

MDL number:

MFCD00001175

Assay:

97%

Form:

powder

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Properties

Quality Level

100

assay

97%

form

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

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Direct target and non-target analysis of urban aerosol sample extracts using atmospheric pressure photoionisation high-resolution mass spectrometry.

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

Determination of oxygen and nitrogen derivatives of polycyclic aromatic hydrocarbons in fractions of asphalt mixtures using liquid chromatography coupled to mass spectrometry with atmospheric pressure chemical ionization.

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

New anthracene-based Schiff bases: Theoretical and experimental investigations of photophysical and electrochemical properties.

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 (