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About This Item
Empirical Formula (Hill Notation):
C8H8N2O2
CAS Number:
Molecular Weight:
164.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
251-158-4
MDL number:
Assay:
97%
InChI key
WJQWYAJTPPYORB-UHFFFAOYSA-N
InChI
1S/C8H8N2O2/c11-10(12)7-1-2-8-6(5-7)3-4-9-8/h1-2,5,9H,3-4H2
SMILES string
[O-][N+](=O)c1ccc2NCCc2c1
assay
97%
mp
92-94 °C (lit.)
functional group
nitro
Application
5-Nitroindoline was used to prepare acetylated glucosylamines using the Suvorov procedure.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Carmine Ostacolo et al.
Journal of medicinal chemistry, 63(1), 163-185 (2019-12-10)
Kv7 K+ channels represent attractive pharmacological targets for the treatment of different neurological disorders, including epilepsy. In this paper, 42 conformationally restricted analogues of the prototypical Kv7 activator retigabine have been synthesized and tested by electrophysiological patch-clamp experiments as Kv7
Substituted glucosylamines containing the indole nucleus.
Magnin AA, et al.
Tetrahedron, 25(18), 4543-4550 (1969)
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