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P11603

Sigma-Aldrich

9-Phenanthrenecarboxaldehyde

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
Beilstein:
511309
EC Number:
225-194-6
MDL number:
MFCD00001175
UNSPSC Code:
12352100
PubChem Substance ID:
24898165
NACRES:
NA.22

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

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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 (

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