Identification | Back Directory | [Name]
TRIMETHYLQUINONE | [CAS]
935-92-2 | [Synonyms]
Cumoquinone psi-Cumoquinone trimethylchinon TRIMETHYLQUINONE Pseudocumoquinone p-Pseudocumoquinone Trimethyl-p-quinone trimethyl-benzoquinon Trimethylbenzoquinone Tocopherol Impurity 12 2,3,5-Trimethylquinone 2,3,5-Tri-methylquinone Cilnidipine Impurity 14 Trimethyl-p-benzoquinone Trimethyl-1,4-benzoquinone 2,3,6-Trimethylbenzoquinone 2,3,5-Trimethylbenzoquinone 2,3,5-trimethyl-p-benzoquinon 2,3,5-Trimethyl-p-benzoquinone 2,3,6-Trimethyl-p-benzoquinone p-Benzoquinone, 2,3,5-trimethyl- 2,3,5-Trimethyl-1,4-benzoquinone 2,5-Dimethyl-3-methyl-1,4-benzoquinone 4-dione,2,3,5-trimethyl-5-cyclohexadien-1 4-dione,2,3,5-trimethyl-5-cyclohexadiene-1 2,3,5-trimethyl-2,5-cyclohexadien-1,4-dione 2,3,5-Trimethyl-2,5-cyclohexadiene-1,4-dione 2,3,5-trimethylcyclohexa-2,5-diene-1,4-dione 5-Cyclohexadiene-1,4-dione,2,3,5-trimethyl-2 2,5-Cyclohexadiene-1,4-dione,2,3,5-triMethyl- | [EINECS(EC#)]
213-309-2 | [Molecular Formula]
C9H10O2 | [MDL Number]
MFCD00045537 | [MOL File]
935-92-2.mol | [Molecular Weight]
150.17 |
Hazard Information | Back Directory | [Chemical Properties]
Yellow crystal | [Uses]
Through a catalytic redox chain ring opening Trimethylquinone can be used to Synthesize Quinone-Containing Carboxylic Acids | [Purification Methods]
Distil the quinone in a vacuum or sublime it in vacuo before use. [Smith et al. J Am Chem Soc 60 318 1939, Beilstein 7 H 161, 7 III 3407, 7 IV 2098.] |
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