9-Anthracenemethanol - ≥98%, used for 9-Anthracenemethanol participates in ring-opening polymerization of L-lactide catalyzed by alumoxane. It undergoes proton exchange reaction with potassium tert-butoxide to yield potassium 9-anthracenemethoxide 9-Anthr

CAS: 1468-95-7 Cat. No.: A101362 Fórmula: C₁₅H₁₂O Peso molecular: 208.26 Beilstein Registry Number: 1873402 Número EC: 215-998-5

GRADE & PURITY ≥98%

Synonyms

anthracen-9-ylmethanol | Anthracene-9-carbinol | 9-anthracene methanol | 9-Hydroxymethylanthracene | NSC 241166 | 9-(Hydroxymethyl)anthracene

Storage

Room temperature

Shipped In

Normal

Descripción general

9-Anthracenemethanol participates in ring-opening polymerization of L-lactide catalyzed by alumoxane. It undergoes proton exchange reaction with potassium tert-butoxide to yield potassium 9-anthracenemethoxide. 9-Anthracenemethanol is a derivative of anthracene used in the Diels-Alder reactions.

Specifications

Sinónimos

anthracen-9-ylmethanol | Anthracene-9-carbinol | 9-anthracene methanol | 9-Hydroxymethylanthracene | NSC 241166 | 9-(Hydroxymethyl)anthracene

Especificaciones y pureza

≥98%

Aplicación

9-Anthracenemethanol participates in ring-opening polymerization of L-lactide catalyzed by alumoxane. It undergoes proton exchange reaction with potassium tert-butoxide to yield potassium 9-anthracenemethoxide 9-Anthracenemethanol was used in the preparat

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488184818
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488184818
• Sonrisas canónicas: C1=CC=C2C(=C1)C=C3C=CC=CC3=C2CO
• IUPAC Name: anthracen-9-ylmethanol
• InChIKey: JCJNNHDZTLRSGN-UHFFFAOYSA-N
• INCHI: 1S/C15H12O/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-9,16H,10H2
• Isómeros SMILES: C1=CC=C2C(=C1)C=C3C=CC=CC3=C2CO
• WGK Alemania: 3
• Peso molecular: 208.26
• Beilstein: 1873402
• Reaxy-Rn: 1873402
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1873402&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Anthracenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Anthracenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Anthracenes
• Alternative Parents: Primary alcohols Hydrocarbon derivatives Aromatic alcohols
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Anthracene - Organic oxygen compound - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Alcohol - Aromatic homopolycyclic compound
• Descripción: 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

Propiedades químicas y físicas

• Solubilidad: Soluble in hot methanol very faint turbidity.Insoluble in water
• Punto de fusión (°C): 158-164°C
• Peso molecular: 208.250 g/mol
• XLogP3: 3.800
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 208.089 Da
• Monoisotopic Mass: 208.089 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 16
• Formal Charge: 0
• Complexity: 216.000
• 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