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经验公式(希尔记法):
C13H9NO
化学文摘社编号:
分子量:
195.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-434-7
Beilstein/REAXYS Number:
7104
MDL number:
Assay:
99%
Form:
solid
InChI key
FZEYVTFCMJSGMP-UHFFFAOYSA-N
InChI
1S/C13H9NO/c15-13-9-5-1-3-7-11(9)14-12-8-4-2-6-10(12)13/h1-8H,(H,14,15)
SMILES string
O=C1c2ccccc2Nc3ccccc13
assay
99%
form
solid
mp
>300 °C (lit.)
λmax
380 nm, 399 nm (2nd)
Quality Level
Gene Information
human ... ABCB1(5243)
Application
9 (10H)-吖啶酮(吖啶酮)用于 9,10-二氢-9-氧代吖啶-10-戊酸甲酯的制备 。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Emerson F Marques et al.
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Environmental pollution (Barking, Essex : 1987), 166, 212-217 (2012-04-21)
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Anton V Dubrovskiy et al.
The Journal of organic chemistry, 77(24), 11232-11256 (2012-12-05)
A novel, efficient route to biologically and pharmaceutically important o-(dimethylamino)aryl ketones, acridones, acridinium salts, and 1H-indazoles has been developed starting from readily available hydrazones of aldehydes and o-(trimethylsilyl)aryl triflates. The reaction proceeds through arynes under mild conditions, tolerates a wide
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