2,6-Diphenylphenol - ≥98% , CAS No.2432-11-3

CAS: 2432-11-3 Cat. No.: D155914 Formula: C₁₈H₁₄O Peso molecolare: 246.31 Beilstein Registry Number: 6(4)5009 Numero EC: 219-401-9

GRADE & PURITY ≥98%

Synonyms

FT-0610721 | 2'-Hydroxy-m-terphenyl | Carbanthrene Printing Flavine GC | AKOS015918243 | DTXSID30947151 | MFCD00009716 | 2,6,-Diphenylphenol | 2,6-Diphenylphenol | 2,6-di-phenylphenol | [1,1':3',1''-Terphenyl]-2'-ol | AMY38633 | D2563 | InChI=1/C18H14O/c1

Storage

Room temperature

Shipped In

Normal

Panoramica

2,6-Diphenylphenol reacts with with (n)BuLi, NaH, KH, or Rb or Cs metal in benzene to yield the solvent-free complexes [M(OAr)]x.
2,6-Diphenylphenol has been used: . as ligand during the synthesis of reduced coordination (less than 6), unchelated manganese oxygen cluster systems. . in the preparation of derivatives of pyrazine-2,3-dicarbonitrile, precursor required for the synthesis of octaazaphthalocyanine (AzaPc) derivatives.

Specifications

Sinonimi

FT-0610721 | 2'-Hydroxy-m-terphenyl | Carbanthrene Printing Flavine GC | AKOS015918243 | DTXSID30947151 | MFCD00009716 | 2,6,-Diphenylphenol | 2,6-Diphenylphenol | 2,6-di-phenylphenol | [1,1':3',1''-Terphenyl]-2'-ol | AMY38633 | D2563 | InChI=1/C18H14O/c1

Specifiche e purezza

≥98%

Condizioni di conservazione di stoccaggio

Room temperature

Spedito in

Normal

Purezza

≥98%

Nomi e identificatori

Pubchem Sid

488185120

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488185120

Sorrisi canonici

C1=CC=C(C=C1)C2=C(C(=CC=C2)C3=CC=CC=C3)O

IUPAC Name

2,6-diphenylphenol

InChIKey

ATGFTMUSEPZNJD-UHFFFAOYSA-N

INCHI

1S/C18H14O/c19-18-16(14-8-3-1-4-9-14)12-7-13-17(18)15-10-5-2-6-11-15/h1-13,19H

Isomeri SMILES

C1=CC=C(C=C1)C2=C(C(=CC=C2)C3=CC=CC=C3)O

Peso molecolare

246.31

Beilstein

6(4)5009

Reaxy-Rn

2051224

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2051224&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Terphenyls

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Terphenyls
• Intermediate Tree Nodes: Not available
• Direct Parent: M-terphenyls
• Alternative Parents: Biphenyls and derivatives 1-hydroxy-4-unsubstituted benzenoids Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Meta-terphenyl - Biphenyl - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as m-terphenyls. These are terphenyls with a structure containing the 1,3-diphenylbenzene skeleton.
• 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

Proprietà chimiche e fisiche

• Punto di fusione (°C): 103 °C
• Peso molecolare: 246.300 g/mol
• XLogP3: 4.800
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 246.104 Da
• Monoisotopic Mass: 246.104 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 237.000
• 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