| Identification | More | [Name]
9-Anthracenemethanol | [CAS]
1468-95-7 | [Synonyms]
9-ANTHRACENEMETHANOL
9-ANTHRACENE METHYL CARBINOL
9-(HYDROXYMETHYL)ANTHRACENE
AKOS B023870
ANTHRACENE-9-METHANOL
ART-CHEM-BB B023870
RARECHEM AL BD 0006
9-Anthracene carbinol
9-Anthrylcarbinol
9-Anthrylmethanol
9-Hydroxymethylantracene
9-Methylolanthracene
anthracene-9-carbinol
9-anthracene carboxylic alcohol
TylosinTartrateBpv2001
9-Anthracenemethanol98%
Anthracene-9-methanol, 98+%
9-Anthracenemethanol 98%
Anthracen-9-ylmethanol | [EINECS(EC#)]
215-998-5 | [Molecular Formula]
C15H12O | [MDL Number]
MFCD00001264 | [Molecular Weight]
208.26 | [MOL File]
1468-95-7.mol |
| Chemical Properties | Back Directory | [Appearance]
light yellow solid | [Melting point ]
162-164 °C(lit.)
| [Boiling point ]
307.46°C (rough estimate) | [density ]
1.0459 (rough estimate) | [refractive index ]
1.5361 (estimate) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Soluble in hot methanol very faint turbidity. | [form ]
Crystalline Powder | [pka]
14.36±0.10(Predicted) | [color ]
Yellow | [Stability:]
Stable. Incompatible with oxidizing agents. | [Detection Methods]
HPLC | [BRN ]
1873402 | [InChIKey]
JCJNNHDZTLRSGN-UHFFFAOYSA-N | [CAS DataBase Reference]
1468-95-7(CAS DataBase Reference) | [NIST Chemistry Reference]
9-Anthracenemethanol(1468-95-7) | [EPA Substance Registry System]
1468-95-7(EPA Substance) |
| Safety Data | Back Directory | [Risk Statements ]
R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [RTECS ]
CB0577500
| [TSCA ]
Yes | [HS Code ]
29062900 | [Toxicity]
mic-bac-sat 390 mmol/L CRNGDP 15,2605,94 |
| Hazard Information | Back Directory | [Chemical Properties]
light yellow solid | [Uses]
An anthracene derivative used in Diels-Alder reactions. Also used in the preparation of 9-anthracenylmethyl-1-piperazinecarboxylate. | [Preparation]
9-Anthracenemethanol is synthesized by hydrogenation of 9-anthracenecarboxaldehyde. It is a versatile precursor to supramolecular assemblies. | [General Description]
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. | [Safety Profile]
Mutation data reported. Whenheated to decomposition it emits acrid smoke andirritating vapors. |
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