Phenanthrene - ≥97% , CAS No.85-01-8

CAS: 85-01-8 Cat. No.: P109245 Summenformel: C14H10 Molekulargewicht: 178.23 Beilstein Registry Number: 1905428 EG-Nummer: 201-581-5
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QUALITÄT & REINHEIT ≥97%
Storage
Argon charged,Room temperature
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Übersicht

Polycyclic aromatic hydrocarbon with three fused benzene rings.

Spezifikationen

Spezifikationen & Reinheit
≥97%
Storage
Argon charged,Room temperature
Verschickt in
Normal
Reinheit
≥97%
Namen und Kennungen
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488179584
Kanonisches Lächeln
C1=CC=C2C(=C1)C=CC3=CC=CC=C32
IUPAC Name
phenanthrene
InChIKey
YNPNZTXNASCQKK-UHFFFAOYSA-N
INCHI
1S/C14H10/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13/h1-10H
Isomere SMILES
C1=CC=C2C(=C1)C=CC3=CC=CC=C32
WGK Deutschland
2
Molekulargewicht
178.23
Beilstein
1905428
Reaxy-Rn
1905428
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1905428&ln=

Erweiterte Daten

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
KlassePhenanthrenes and derivatives
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPhenanthrenes and derivatives
Alternative Parents Naphthalenes  Aromatic hydrocarbons  Polycyclic hydrocarbons  Unsaturated hydrocarbons  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Phenanthrene - Naphthalene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as phenanthrenes and derivatives. These are polycyclic compounds containing a phenanthrene moiety, which is a tricyclic aromatic compound with three non-linearly fused benzene.
External Descriptors a ring
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CXCL8 Tchem Interleukin-8 (642 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2A6 Tchem Cytochrome P450 2A6 (2861 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THP-1 (11052 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCT-116 (91556 Activities)
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Lymphoblastoid cell (5959 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
Cyp2a5 Cytochrome P450 2A5 (126 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nannizzia gypsea (2039 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Microsporum canis (872 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus flavus (8875 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus niger (16508 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Saccharomyces cerevisiae (19171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus fumigatus (16427 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichophyton rubrum (3646 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Epidermophyton floccosum (561 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichophyton mentagrophytes (4846 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

24 results found

Lot NumberCertificate TypeDatumArtikel
L2406132L2406132Certificate of AnalysisSep 01, 2026 P109245
B2308468B2308468Certificate of AnalysisAug 03, 2026 P109245
B2308373B2308373Certificate of AnalysisAug 03, 2026 P109245
C2604673C2604673Certificate of AnalysisJan 29, 2026 P109245
C2604675C2604675Certificate of AnalysisJan 29, 2026 P109245
C2604677C2604677Certificate of AnalysisJan 29, 2026 P109245
K2520425K2520425Certificate of AnalysisOct 31, 2025 P109245
K2520448K2520448Certificate of AnalysisOct 31, 2025 P109245
K2520449K2520449Certificate of AnalysisOct 31, 2025 P109245
F2505543F2505543Certificate of AnalysisMay 13, 2025 P109245
F2505544F2505544Certificate of AnalysisMay 13, 2025 P109245
F2505542F2505542Certificate of AnalysisMay 13, 2025 P109245
L2403095L2403095Certificate of AnalysisDec 05, 2024 P109245
F2506638F2506638Certificate of AnalysisJul 08, 2024 P109245
I2124346I2124346Certificate of AnalysisJul 10, 2023 P109245
I2124344I2124344Certificate of AnalysisJul 10, 2023 P109245
I2124345I2124345Certificate of AnalysisJul 10, 2023 P109245
G2222703G2222703Certificate of AnalysisJun 17, 2022 P109245
H2312228H2312228Certificate of AnalysisJun 17, 2022 P109245
G2222705G2222705Certificate of AnalysisJun 17, 2022 P109245
G2222704G2222704Certificate of AnalysisJun 17, 2022 P109245
A2423089A2423089Certificate of AnalysisJun 17, 2022 P109245
D2324732D2324732Certificate of AnalysisJun 17, 2022 P109245
A2423357A2423357Certificate of AnalysisJun 17, 2022 P109245
Chemische und physikalische Eigenschaften
LöslichkeitSoluble in alcohol, benzene, ether, chloroform, toluene and glacial acetic acid. Insoluble in water.
EmpfindlichkeitLight sensitive
Flammpunkt (°F)-0.4℉
Flammpunkt (°C)-18 °C
Siedepunkt (°C)340°C
Schmelzpunkt (°C)100°C
Molekulargewicht178.230 g/mol
XLogP34.500
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count0
Exact Mass178.078 Da
Monoisotopic Mass178.078 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count14
Formal Charge0
Complexity174.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
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