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About This Item
Empirical Formula (Hill Notation):
C8H8N2O2
CAS Number:
Molecular Weight:
164.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
mp
92-94 °C (lit.)
functional group
nitro
SMILES string
[O-][N+](=O)c1ccc2NCCc2c1
InChI
1S/C8H8N2O2/c11-10(12)7-1-2-8-6(5-7)3-4-9-8/h1-2,5,9H,3-4H2
InChI key
WJQWYAJTPPYORB-UHFFFAOYSA-N
Application
5-Nitroindoline was used to prepare acetylated glucosylamines using the Suvorov procedure.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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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