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 Formule: C₁₅H₁₂O Poids moléculaire: 208.26 Beilstein Registry Number: 1873402 Numéro CE: 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

Vue d’ensemble

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

Synonymes

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

Spécifications et pureté

≥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

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Pureté

≥98%

Noms et identifiants

Pubchem Sid

488184818

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488184818

Sourires canoniques

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

Isomères SMILES

C1=CC=C2C(=C1)C=C3C=CC=CC3=C2CO

WGK Allemagne

3

Poids moléculaire

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
    • Classe Anthracenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: 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

Propriétés chimiques et physiques

• Solubilité: Soluble in hot methanol very faint turbidity.Insoluble in water
• Point de fusion (°C): 158-164°C
• Poids moléculaire: 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