N1607
1,8-萘二甲酸酐
别名:
萘并[1,8,8 A - C ， D ]吡喃-1,3-二酮
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关于此项目
经验公式（希尔记法）:
C12H6O3
化学文摘社编号:
分子量:
198.17
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
201-380-2
Beilstein/REAXYS Number:
153190
MDL number:
InChI key
GRSMWKLPSNHDHA-UHFFFAOYSA-N
InChI
1S/C12H6O3/c13-11-8-5-1-3-7-4-2-6-9(10(7)8)12(14)15-11/h1-6H
SMILES string
O=C1OC(=O)c2cccc3cccc1c23
form
powder
mp
267-269 °C (lit.)
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
521.6 °F
flash_point_c
272 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
危险化学品
此项目有
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 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
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