Xanthone - 10mM in DMSO , CAS No.90-47-1

CAS: 90-47-1 Cat. No.: X426849 Summenformel: C13H8O2 Molekulargewicht: 196.2 Beilstein Registry Number: 140443 EG-Nummer: 201-997-7 PubChem CID: 7020
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GRADE & PURITY 10mM in DMSO
Synonyms
F15407 | AI3-00077 | EN300-20176 | SMR000112239 | NCGC00095484-03 | 9H-Xanthen-9-one | NSC-14978 | Xanthene, 9-oxo- | Q421789 | BDBM50155411 | A843557 | NSC 14978 | Xanthen-9-one | Dibenzo-gamma-pyrone | MLS002207109 | NCGC00095484-01 | SPECTRUM200523 | S
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
Size
Deutschland (EU)
USA*
Price
Qty
1ml
X426849-1ml
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38,96€

58,92€
Speichern 19,96 € (33.87%)
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

application:

Xanthone is used predominantly as oxygenated polycyclic aromatic compounds, and as a vasorelaxant. It can be used as a fluorescent agent, as well as an intermediate in organic synthesis and chemical research.

Specifications

Synonyme
F15407 | AI3-00077 | EN300-20176 | SMR000112239 | NCGC00095484-03 | 9H-Xanthen-9-one | NSC-14978 | Xanthene, 9-oxo- | Q421789 | BDBM50155411 | A843557 | NSC 14978 | Xanthen-9-one | Dibenzo-gamma-pyrone | MLS002207109 | NCGC00095484-01 | SPECTRUM200523 | S
Spezifikationen & Reinheit
10mM in DMSO
Storage
Store at -80°C
Verschickt in
Dry ice packs + Cold packs
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Aktionsart
INHIBITOR
Namen und Kennungen
Pubchem Sid528770325
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/528770325
Kanonisches LächelnC1=CC=C2C(=C1)C(=O)C3=CC=CC=C3O2
IUPAC Namexanthen-9-one
InChIKeyJNELGWHKGNBSMD-UHFFFAOYSA-N
INCHI1S/C13H8O2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1-8H
Isomere SMILES C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3O2
WGK Deutschland 3
RTECS ZD5711000
PubChem CID 7020
UN-Nummer 2811
Molekulargewicht 196.2
Beilstein 140443
Reaxy-Rn 140443

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
KlasseBenzopyrans
Subclass1-benzopyrans
Intermediate Tree Nodes Dibenzopyrans - Xanthenes
Direct ParentXanthones
Alternative Parents Chromones  Pyranones and derivatives  Benzenoids  Heteroaromatic compounds  Oxacyclic compounds  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Xanthone - Chromone - Pyranone - Benzenoid - Pyran - Heteroaromatic compound - Oxacycle - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.
External Descriptors xanthones
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
PGAM1 Tchem Phosphoglycerate mutase 1 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MAOA Tclin Amine oxidase [flavin-containing] A (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLA Tclin Alpha-galactosidase A (5444 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CASP1 Tchem Caspase-1 (6235 Activities)
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CASP7 Tchem Caspase-7 (3146 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
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DU-145 (51482 Activities)
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HeLa (62764 Activities)
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SMN1 Tchem Survival motor neuron protein (34246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGAM1 Tchem Phosphoglycerate mutase 1 (143 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
Hdac6 Histone deacetylase 6 (222 Activities)
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Spodoptera frugiperda (784 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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Drechslera (102 Activities)
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Fusarium oxysporum f. sp. vasinfectum (242 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemische und physikalische Eigenschaften
Siedepunkt (°C)349-350°C
Schmelzpunkt (°C)172-180℃
Molekulargewicht196.200 g/mol
XLogP33.400
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass196.052 Da
Monoisotopic Mass196.052 Da
Topological Polar Surface Area26.300 Ų
Heavy Atom Count15
Formal Charge0
Complexity237.000
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
FAQs und Artikel
Citations of This Product
Referenzen
1. Nian Wang, Die Zhou, Huaying Liu, Yina Tu, Yanqiong Ma, Yingjie Li.  (2023)  Triplet-Excited Dissolved Organic Matter Efficiently Promoted Atmospheric Sulfate Production: Kinetics and Mechanisms.  Separations,  10  (6): (335).  [PMID:] [10.3390/separations10060335]
2. Huan He, Dan Xiong, Fengxia Han, Zhiang Xu, Bin Huang, Xuejun Pan.  (2018)  Dissolved oxygen inhibits the promotion of chlorothalonil photodegradation mediated by humic acid.  JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY,      [PMID:] [10.1016/j.jphotochem.2018.04.050]
3. Mingye Zhao, Jie Chen, Heyong Wang, Yuqing Wang, Guixiang Huang, Ning Zhu, Yuguang Li, Zheng Fang, Yujing Hu, Kai Guo.  (2024)  A Photo-Enzymatic Cascade to Access Dihydrocoumarins from Incompatibility to Compatibility.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2024.113852]
Lösungsrechner
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