Identification | More | [Name]
2-Methyl anthraquinone | [CAS]
84-54-8 | [Synonyms]
2-Methyl-9,10-anthracenedione 2-METHYLANTHRAQUINONE 2-METHYL AQ LABOTEST-BB LT00159669 Methylanthraquinone METHYLANTHRAQUINONE, 2- TECTOQUINONE 2-methyl-10-anthracenedione 2-methyl-9,10(9H,10H)-anthracenedione 2-Methylanthra-9,10-quinone 2-Methylanthracenedione 2-Methylanthrapuinone 9,10-Anthracenedione,2-methyl- 9,10-Antracenedione, 2-methyl- Anthraquinone, 2-methyl- anthraquinone,2-methyl- beta-Methylanthraquinone -Methylanthranpuinone Techtoquinone Tectochinon | [EINECS(EC#)]
201-539-6 | [Molecular Formula]
C15H10O2 | [MDL Number]
MFCD00001235 | [Molecular Weight]
222.24 | [MOL File]
84-54-8.mol |
Chemical Properties | Back Directory | [Appearance]
YELLOW TO GREEN-YELLOW FINE POWDER | [Melting point ]
170-173 °C (lit.) | [Boiling point ]
236-238 °C/10 mmHg (lit.) | [density ]
1.1404 (rough estimate) | [vapor pressure ]
0Pa at 25℃ | [refractive index ]
1.6600 (estimate) | [Fp ]
209 °C
| [storage temp. ]
2-8°C | [solubility ]
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | [form ]
powder to crystal | [color ]
Light orange to Yellow to Green | [Water Solubility ]
Soluble in water 1.234 mg/L @ 25°C. | [Merck ]
14,6021 | [BRN ]
2050523 | [InChIKey]
NJWGQARXZDRHCD-UHFFFAOYSA-N | [LogP]
3.4 at 25℃ | [Uses]
Organic synthesis. | [CAS DataBase Reference]
84-54-8(CAS DataBase Reference) | [NIST Chemistry Reference]
9,10-Anthracenedione, 2-methyl-(84-54-8) | [EPA Substance Registry System]
84-54-8(EPA Substance) |
Safety Data | Back Directory | [Hazard Codes ]
Xi,N | [Risk Statements ]
R51/53:Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment . | [Safety Statements ]
S22:Do not breathe dust . S24/25:Avoid contact with skin and eyes . S61:Avoid release to the environment. Refer to special instructions safety data sheet . | [RIDADR ]
UN 3077 9/PG 3 | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [TSCA ]
Yes | [HS Code ]
29146990 |
Hazard Information | Back Directory | [Chemical Properties]
YELLOW TO GREEN-YELLOW FINE POWDER | [Definition]
ChEBI: An anthraquinone that is 9,10-anthraquinone in which the hydrogen at position 2 is substituted by a methyl group. | [Reactions]
The compound is produced by the reaction of phthalic anhydride and toluene. It can be chlorinated to give 1-chloro-2-methylanthraquinone. Nitration gives 1-nitro-2-methylanthraquinone, which can be reduced to 1-amino-2-methyl derivative. Oxidation of the methyl group gives anthraquinone-2-carboxylic acid. | [Synthesis Reference(s)]
Canadian Journal of Chemistry, 44, p. 2881, 1966 DOI: 10.1139/v66-428 | [Synthesis Reference(s)]
Organic Syntheses, Coll. Vol. 1, p. 353, 1941 Tetrahedron Letters, 24, p. 5499, 1983 DOI: 10.1016/S0040-4039(00)94122-4 | [Flammability and Explosibility]
Notclassified | [Purification Methods]
Crystallise the quinone from EtOH, then sublime it. It has max at 257, 275 and 330nm (EtOH). [Hersbery & Fieser J Am Chem Soc 63 2562 1941, Beilstein 7 H 809, 7 III 4104, 7 IV 2574.] |
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