N1607
1,8-Naphthalic anhydride
Sinonimo/i:
Naphtho[1,8,8a-c,d]pyran-1,3-dione
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About This Item
Formula empirica (notazione di Hill):
C12H6O3
Numero CAS:
Peso molecolare:
198.17
Beilstein:
153190
Numero CE:
Numero MDL:
Codice UNSPSC:
12162002
ID PubChem:
NACRES:
NA.23
Prodotti consigliati
Forma fisica
powder
Livello qualitativo
Punto di fusione
267-269 °C (lit.)
Stringa SMILE
O=C1OC(=O)c2cccc3cccc1c23
InChI
1S/C12H6O3/c13-11-8-5-1-3-7-4-2-6-9(10(7)8)12(14)15-11/h1-6H
GRSMWKLPSNHDHA-UHFFFAOYSA-N
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Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
521.6 °F
Punto d’infiammabilità (°C)
272 °C
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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C Gaillard et al.
FEBS letters, 352(2), 219-221 (1994-09-26)
In plants potentially toxic compounds are ultimately deposited in the large central vacuole. In this report we show that isolated barley mesophyll vacuoles take up the glucoside conjugate of the herbicide derivate [5-hydroxyphenyl]primisulfuron. Transport is stimulated by Mg-ATP and is
Lijuan Xie et al.
Bioorganic & medicinal chemistry, 17(2), 804-810 (2008-12-17)
A series of 5-alkylamino substituted amonafide analogues were synthesized from naphthalic anhydride by three steps including bromization, amination and CuI/proline catalyzed coupling reaction. The CuI/L-proline catalyzed coupling reaction was first applied to the naphthalimide system. These new amonafide analogues showed
Nikolai I Georgiev et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 183, 7-16 (2017-04-23)
Two novel highly water-soluble fluorescence sensing 1,8-naphthalimides are synthesized and investigated. The novel compounds are designed on the "fluorophore-receptor
J J McFadden et al.
Biochemical and biophysical research communications, 168(1), 206-213 (1990-04-16)
In vitro metabolism of the herbicide bentazon was studied in microsomal membranes isolated from 6-day-old etiolated corn shoots. Microsomes isolated from shoots of nontreated seeds did not metabolize bentazon when assayed with NADPH or peroxides. However, microsomes isolated from shoots
Jean Camps et al.
American journal of dentistry, 15(5), 300-304 (2003-01-23)
To compare in vitro the efficacy of five resin-based desensitizing agents at reducing human dentin permeability and to compare their cytotoxicity. The tested hypothesis was that their different curing techniques cause variations in efficiency and cytotoxicity. Dentin slices (0.5 +/-
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