9,10-Dihydroanthracene - ≥98%(GC) , CAS No.613-31-0

CAS: 613-31-0 Cat. No.: D155012 Formule: C₁₄H₁₂ Poids moléculaire: 180.25 Beilstein Registry Number: 1364580 Numéro CE: 210-336-1

GRADE & PURITY ≥98%(GC)

Synonyms

AI3-09026 | 9,10-Dihydroanthracene, 97% | NSC30805 | NSC-30805 | AKOS004907975 | Z142C238GB | BDBM50060852 | D0549 | 9,10-DIHYDROANTHRACENE | 9,10-Dihydro-anthracene | FT-0621599 | MFCD00001239 | NSC 30805 | UNII-Z142C238GB | DTXSID3075256 | STK365298 | D

Storage

Room temperature

Shipped In

Normal

Vue d’ensemble

9,10-Dihydroanthracene causes the transfer hydrogenation of C60 and C70 in the presence of 7Hbenzanthrene catalyst. It was oxidatively aromatized to the corresponding anthracene in the presence of molecular oxygen as an oxidant and activated carbon as a promoter in xylene.

Specifications

Synonymes

AI3-09026 | 9,10-Dihydroanthracene, 97% | NSC30805 | NSC-30805 | AKOS004907975 | Z142C238GB | BDBM50060852 | D0549 | 9,10-DIHYDROANTHRACENE | 9,10-Dihydro-anthracene | FT-0621599 | MFCD00001239 | NSC 30805 | UNII-Z142C238GB | DTXSID3075256 | STK365298 | D

Spécifications et pureté

≥98%(GC)

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Pureté

≥98%(GC)

Noms et identifiants

Pubchem Sid

488181488

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488181488

Sourires canoniques

C1C2=CC=CC=C2CC3=CC=CC=C31

IUPAC Name

9,10-dihydroanthracene

InChIKey

WPDAVTSOEQEGMS-UHFFFAOYSA-N

INCHI

1S/C14H12/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-8H,9-10H2

Isomères SMILES

C1C2=CC=CC=C2CC3=CC=CC=C31

WGK Allemagne

3

Poids moléculaire

180.25

Beilstein

1364580

Reaxy-Rn

1364575

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1364575&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Anthracenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Anthracenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Anthracenes
• Alternative Parents: Aromatic hydrocarbons Polycyclic hydrocarbons Unsaturated hydrocarbons
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Anthracene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound
• Description: This compound belongs to the class of organic compounds known as anthracenes. These are organic compounds containing a system of three linearly fused benzene rings.
• 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

Cibles associées (humaines)

ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)

Discover Target: ALOX5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mécanismes d'action

Propriétés chimiques et physiques

• Point d'ébullition (°C): 313 °C
• Point de fusion (°C): 103-107℃
• Poids moléculaire: 180.240 g/mol
• XLogP3: 4.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 180.094 Da
• Monoisotopic Mass: 180.094 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 154.000
• 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