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| | Acenaphthenequinone Basic information |
| Product Name: | Acenaphthenequinone | | Synonyms: | Acenaphthenequinone;1,2-Acenaphthenedione;ACQ;ACENAPHTHENCHINON TECHN.;ACENAPHTHENEQUINONE 97+%;Acenaphthenequinone, tech., 95%;acenaphthene-1,2-dione;2,4-Dioxy-3,3-diethyl-5-methylpiperidine;3,3-Diethyl-2,4-dioxo-5-methylpiperidine;3,3-Diethyl-5-methyl-2,4-piperidinedione | | CAS: | 82-86-0 | | MF: | C12H6O2 | | MW: | 182.17 | | EINECS: | 201-441-3 | | Product Categories: | Pharmaceutical Intermediates;Anthraquinones, Hydroquinones and Quinones;C11 to C12;C11 to C12G Proteins and Cyclic Nucleotides;Cyclic Nucleotide Metabolism;Guanylyl Cyclase Inhibitors;Carbonyl Compounds;Ketones | | Mol File: | 82-86-0.mol |  |
| | Acenaphthenequinone Chemical Properties |
| | Acenaphthenequinone Usage And Synthesis |
| Chemical Properties | ochre powder and granules | | Uses | Acenaphthenequinone is used in the preparation of acetylcholinesterase inhibitory agents. It is also used in the preparation of turn-on sensors for cysteine/homocysteine and its application in bioimaging. Further, it is used as an intermediate in manufacturing of dyes and pharmaceuticals. In addition to this, it is used in chemical research as a drug and therapeutic agent. | | Definition | ChEBI: A member of the class of orthoquinones that is the 1,2-dioxo derivative of acenaphthene. | | Safety Profile | Moderately toxic by an unspecifiedroute. When heated to decomposition it emits acrid smokeand irritating vapors. | | Purification Methods | Extract it with, then recrystallise it twice from *C6H6. Dry it in vacuo. [LeFevre et al. J Chem Soc 974 1963, Beilstein 7 IV 2498.] |
| | Acenaphthenequinone Preparation Products And Raw materials |
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