Identification | More | [Name]
Acenaphthenequinone | [CAS]
82-86-0 | [Synonyms]
1,2-ACENAPHTHYLENEDIONE 1,2-DIHYDROACENAPHTHYLENEQUINONE 1,2-diketoacenaphthene 1,2-DIOXOACENAPHTHENE ACENAPHTHAQUINONE ACENAPHTHENEQUINONE ACENAPHTHEQUINONE ACENAPHTHOQUINONE ACENAPHTHYLENE-1,2-DIONE AKOS 92207 NAPHTHYLENEETHYLENEQUINONE PERI-ETHYENENAPHTHALENEQUINONE 1,2-Acenaphthalenedione 1,2-Acenaphthenedione 1,2-Acenaphthenequinone Acenaphthenedione acenaphthylene-1,2-quinone acenaphthylenequinone Acenaphthenequinone 1,2-Acenaphthenedione ACQ ACQ | [EINECS(EC#)]
201-441-3 | [Molecular Formula]
C12H6O2 | [MDL Number]
MFCD00003805 | [Molecular Weight]
182.17 | [MOL File]
82-86-0.mol |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . S37/39:Wear suitable gloves and eye/face protection . | [RIDADR ]
UN 2920 | [WGK Germany ]
3
| [RTECS ]
AB1024500
| [TSCA ]
Yes | [HS Code ]
29146990 | [Hazardous Substances Data]
82-86-0(Hazardous Substances Data) | [Toxicity]
LD50 unr-rat: 728 mg/kg RPTOAN 41,146,78 |
Hazard Information | Back Directory | [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.] |
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