10-Phenyl-9(10H)-acridone - ≥98%(HPLC) , CAS No.5472-23-1

CAS: 5472-23-1 Cat. No.: P404909 Molecular Weight: 271.32 EC Number: 878-853-0 PubChem CID: 138522

GRADE & PURITY ≥98%(HPLC)

Synonyms

10-Phenyl-9(10H)-acridone | T72601 | 10-PHENYL-9,10-DIHYDROACRIDIN-9-ONE | 9-Acridanone, 10-phenyl- | 9-Hydro-9-oxo-10-phenylacridine | Phenylacridone | 10-Phenyl-9(10H)-acridinone, 95% | 10-Phenylacridin-9(10H)-one | 9(10H)-Acridinone, 10-phenyl- | SR-01

Storage

Room temperature

Overview

Maximum Absorption Wavelength:394(CH3CN)nm

Application：

Substrate was reported in the synthesis of oxirane derivatives through a two-step synthesis involving a McMurray reaction with 2-Adamantanone.

Specifications

Synonyms

10-Phenyl-9(10H)-acridone | T72601 | 10-PHENYL-9, 10-DIHYDROACRIDIN-9-ONE | 9-Acridanone, 10-phenyl- | 9-Hydro-9-oxo-10-phenylacridine | Phenylacridone | 10-Phenyl-9(10H)-acridinone, 95% | 10-Phenylacridin-9(10H)-one | 9(10H)-Acridinone, 10-phenyl- | SR-01

Specifications & Purity

≥98%(HPLC)

Storage

Room temperature

Purity

≥98%(HPLC)

Names and Identifiers

• Pubchem Sid: 488188003
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488188003
• Canonical Smiles: C1=CC=C(C=C1)N2C3=CC=CC=C3C(=O)C4=CC=CC=C42
• IUPAC Name: 10-phenylacridin-9-one
• InChIKey: GOKIEMZASYETFM-UHFFFAOYSA-N
• INCHI: 1S/C19H13NO/c21-19-15-10-4-6-12-17(15)20(14-8-2-1-3-9-14)18-13-7-5-11-16(18)19/h1-13H
• Isomeric SMILES: C1=CC=C(C=C1)N2C3=CC=CC=C3C(=O)C4=CC=CC=C42
• PubChem CID: 138522
• Molecular Weight: 271.32
• Reaxy-Rn: 208042

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Quinolines and derivatives
      • Subclass Phenylquinolines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Quinolines and derivatives
• Subclass: Phenylquinolines
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenylquinolines
• Alternative Parents: Acridones Hydroquinolones Hydroquinolines Pyridines and derivatives Benzene and substituted derivatives Vinylogous amides Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Phenylquinoline - Acridone - Acridine - Benzoquinoline - Dihydroquinolone - Dihydroquinoline - Monocyclic benzene moiety - Pyridine - Benzenoid - Heteroaromatic compound - Vinylogous amide - Azacycle - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
• Description: This compound belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Melt Point(°C): 275 °C
• Molecular Weight: 271.300 g/mol
• XLogP3: 4.700
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 271.1 Da
• Monoisotopic Mass: 271.1 Da
• Topological Polar Surface Area: 20.300 Ų
• Heavy Atom Count: 21
• Formal Charge: 0
• Complexity: 361.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1