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Merck
CN

P11603

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
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

Key Documents

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Product Name

9-Phenanthrenecarboxaldehyde, 97%

InChI key

QECIGCMPORCORE-UHFFFAOYSA-N

InChI

1S/C15H10O/c16-10-12-9-11-5-1-2-6-13(11)15-8-4-3-7-14(12)15/h1-10H

SMILES string

[H]C(=O)c1cc2ccccc2c3ccccc13

assay

97%

form

powder

mp

100-103 °C (lit.)

Quality Level

100

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Related Categories

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB0641
STBL1018
STBK9958
STBK0841
STBJ9042

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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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