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 Formula: C₁₅H₁₂O Molecular Weight: 208.26 Beilstein Registry Number: 1873402 EC Number: 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

Overview

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

Synonyms

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

Specifications & Purity

≥98%

Application

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

Storage

Room temperature

Shipped In

Normal

Purity

≥98%

Names and Identifiers

• Pubchem Sid: 488184818
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488184818
• Canonical Smiles: 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
• Isomeric SMILES: C1=CC=C2C(=C1)C=C3C=CC=CC3=C2CO
• WGK Germany: 3
• Molecular Weight: 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
    • Class Anthracenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: 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
• 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

Chemical and Physical Properties

• Solubility: Soluble in hot methanol very faint turbidity.Insoluble in water
• x_melt_point_char: 158-164°C
• Molecular Weight: 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