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N1607

Sigma-Aldrich

1,8-Naphthalic anhydride

Sinónimos:

Naphtho[1,8,8a-c,d]pyran-1,3-dione

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About This Item

Fórmula empírica (notación de Hill):
C12H6O3
Número de CAS:
81-84-5
Peso molecular:
198.17
Beilstein/REAXYS Number:
153190
EC Number:
201-380-2
MDL number:
MFCD00006925
UNSPSC Code:
12162002
PubChem Substance ID:
24897503
NACRES:
NA.23

form

powder

mp

267-269 °C (lit.)

SMILES string

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

InChI key

GRSMWKLPSNHDHA-UHFFFAOYSA-N

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

521.6 °F

flash_point_c

272 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Stacey Sova et al.
Photochemistry and photobiology, 95(5), 1169-1178 (2019-04-18)
The ground- and excited-state interactions of β-alanine, tyrosine and l-dopa substituted 1,8 naphthalimides (NI-Ala, NI-Tyr and NI-Dopa) with lysozyme and mushroom tyrosinase were evaluated to understand the mechanism of oxidative modification. Photooxidative cross-linking of lysozyme was observed for all three
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 +/-
J Sauther et al.
The Journal of chemical physics, 131(3), 034711-034711 (2009-07-25)
The pi-conjugated organic molecules 3,4,9,10-perylene-tetracarboxylic dianhydride, 1,4,5,8-naphthalene-tetracarboxylic dianhydride, and 1,8-naphthalene-dicarboxylic anhydride were investigated via gas phase and bulk ultraviolet photoemission spectroscopy and compared to density functional theory calculations. Values for final state effects such as intermolecular polarization were determined and
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
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
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