Coronene - ≥97% , CAS No.191-07-1

CAS: 191-07-1 Cat. No.: C119985 Molecular Weight: 300.35 Beilstein Registry Number: 658468 EC Number: 205-881-7

GRADE & PURITY ≥97%

Synonyms

Coronene 10 microg/mL in Acetonitrile | Dibenzo[ghi,pqr]perylene | Q420614 | Coronene, BCR(R) certified Reference Material | J-012345 | SY051583 | NSC90725 | NSC-90725 | OL10162 | CCRIS 908 | EINECS 205-881-7 | ACETICACID2-ACETOXY-5-ACETYL-PHENYLESTER | 1

Storage

Store at 2-8°C

Shipped In

Wet ice

Overview

Product Application:

Coronene can be used：To synthesize active materials for organic photovoltaic and optoelectronic applications.As ′nucleation seed′ to synthesize graphene by vapor deposition at low temperatures.To build novel polycyclic aromatic molecular frameworks and architectures.

Specifications

Synonyms

Coronene 10 microg/mL in Acetonitrile | Dibenzo[ghi, pqr]perylene | Q420614 | Coronene, BCR(R) certified Reference Material | J-012345 | SY051583 | NSC90725 | NSC-90725 | OL10162 | CCRIS 908 | EINECS 205-881-7 | ACETICACID2-ACETOXY-5-ACETYL-PHENYLESTER | 1

Specifications & Purity

≥97%

Storage

Store at 2-8°C

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥97%

Names and Identifiers

• Canonical Smiles: C1=CC2=C3C4=C1C=CC5=C4C6=C(C=C5)C=CC7=C6C3=C(C=C2)C=C7
• IUPAC Name: coronene
• InChIKey: VPUGDVKSAQVFFS-UHFFFAOYSA-N
• INCHI: 1S/C24H12/c1-2-14-5-6-16-9-11-18-12-10-17-8-7-15-4-3-13(1)19-20(14)22(16)24(18)23(17)21(15)19/h1-12H
• Isomeric SMILES: C1=CC2=C3C4=C1C=CC5=C4C6=C(C=C5)C=CC7=C6C3=C(C=C2)C=C7
• WGK Germany: 3
• RTECS: GM5400000
• Molecular Weight: 300.35
• Beilstein: 658468
• Reaxy-Rn: 658468
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=658468&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Class Pyrenes
      • Subclass Benzopyrenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: Pyrenes
• Subclass: Benzopyrenes
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzopyrenes
• Alternative Parents: Triphenylenes Anthracenes Aromatic hydrocarbons Polycyclic hydrocarbons Unsaturated hydrocarbons
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Benzo-e-pyrene - Triphenylene - Phenanthrene - Anthracene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound
• Description: This compound belongs to the class of organic compounds known as benzopyrenes. These are organic compounds containing a benzene fused to a pyrene(benzo[def]phenanthrene) ring system.
• External Descriptors: ortho- and peri-fused polycyclic arene

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

• Solubility: Insoluble in water
• Sensitivity: Light sensitive
• Boil Point(°C): 525°C
• Melt Point(°C): 440°C
• Molecular Weight: 300.400 g/mol
• XLogP3: 7.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 300.094 Da
• Monoisotopic Mass: 300.094 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 24
• Formal Charge: 0
• Complexity: 376.000
• 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

References

1. Yan Liu, Changmin Zhang, Kangle Ding, Zhenzhen Yu, Yi Wu.  (2022)  Thermochemical Sulfate Reduction by Pyrobitumen: Review and Experiments.  ACS Earth and Space Chemistry,      [PMID:] [10.1021/acsearthspacechem.1c00291]

2. Rui-Ling Zhang, Yang Yang, Song-Qiu Yang, Ke-Li Han.  (2017)  Unveiling excited state energy transfer and charge transfer in a host/guest coordination cage.  PHYSICAL CHEMISTRY CHEMICAL PHYSICS,  20  (4): (2205-2210).  [PMID:29264601] [10.1039/C7CP06577A]