| Identification | More | [Name]
3-NITRO-1,8-NAPHTHALIC ANHYDRIDE | [CAS]
3027-38-1 | [Synonyms]
3-NITRO-1,8-NAPHTHALIC ANHYDRIDE
1H,3H-Naphtho(1,8-cd)pyran-1,3-dione, 5-nitro-
3h-naphtho(1,8-cd)pyran-1,3-dione,5-nitro-1
3-Nitronaphthalic anhydride
3-nitro-naphthalicanhydrid
5-Nitro-1H,3H-benzo[de]isochromene-1,3-dione
Naphthalic anhydride, 3-nitro-
3-NITRO-1,8-NAPHTHALIC ANHYDRIDE, TECH.
5-NITRO-BENZO[DE]ISOCHROMENE-1,3-DIONE
3-nitronaphthalene-1,8-dicarboxylic anhydride
3-NITRO-1,8-NAPHTHALIC ANHYDRIDE 99%
3-Nitro-1,8-naphthalenedicarboxylic anhydride | [EINECS(EC#)]
201-380-2 | [Molecular Formula]
C12H5NO5 | [MDL Number]
MFCD00006926 | [Molecular Weight]
243.17 | [MOL File]
3027-38-1.mol |
| Chemical Properties | Back Directory | [Appearance]
Light yellow to beige or light brown powder | [Melting point ]
247-249 °C (dec.) (lit.) | [Boiling point ]
386.04°C (rough estimate) | [density ]
1.4429 (rough estimate) | [refractive index ]
1.4500 (estimate) | [storage temp. ]
Inert atmosphere,2-8°C | [solubility ]
DMSO (Slightly), Methanol (Slightly, Heated, Sonicated) | [form ]
Powder | [color ]
Light yellow to beige or light brown | [BRN ]
23762 | [CAS DataBase Reference]
3027-38-1(CAS DataBase Reference) |
| 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 . | [WGK Germany ]
3
| [RTECS ]
QK5370000
| [F ]
10-21 | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29163900 |
| Hazard Information | Back Directory | [Chemical Properties]
Light yellow to beige or light brown powder | [Uses]
3-Nitro-1,8-naphthalic anhydride is a reagent used to synthesize a monoboronic acid fluorescent sensor that exhibits emission suitable for ratiometric testing and also displays sensitivity for glucose relative to fructose and galactose. 3-Nitro-1,8-naphthalic anhydride is also used as a starting reagent in the synthesis of 5-substituted naphthalimide derivatives which exhibit high anti-cancer activity. |
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