344214
2-Bromo-3′-nitroacetophenone
97%
Synonym(s):
3′-Nitrophenacyl bromide
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About This Item
Linear Formula:
O2NC6H4COCH2Br
CAS Number:
Molecular Weight:
244.04
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
218-764-0
MDL number:
Assay:
97%
Form:
solid
InChI key
GZHPNIQBPGUSSX-UHFFFAOYSA-N
InChI
1S/C8H6BrNO3/c9-5-8(11)6-2-1-3-7(4-6)10(12)13/h1-4H,5H2
SMILES string
[O-][N+](=O)c1cccc(c1)C(=O)CBr
assay
97%
form
solid
mp
90-96 °C (lit.)
functional group
bromo, ketone, nitro
Quality Level
Related Categories
Application
2-Bromo-3′-nitroacetophenone may be used in the preparation of 2-bromo-3′-nitroacetophenone. It may be used in the preparation of 2-hydroxy-ethyl-1-[(3-nitro-phenyl)-2-oxoethyl]-piperidinium bromide.
General description
Debromination of 2-bromo-3′-nitroacetophenone in various solvents has been reported.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Debromination of a-Bromoketones and vic-Dibromides Using a NaI/Na2SO3 System.
Lee SH, et al.
Bull. Korean Chem. Soc., 25(11), 1723-1723 (2004)
Sarwat Jahan et al.
Pakistan journal of pharmaceutical sciences, 26(3), 517-523 (2013-04-30)
Synthesis of novel phenacyl derivatives of alkyl piperidine as cytotoxic agents via simple and single step reaction procedure is going to be reported here. Twelve new compounds were successfully synthesized in moderate yield and in solid form. Their synthesis was
3-Aryl-1, 2-dihydroquinoxalines.
Figueras J.
The Journal of Organic Chemistry, 31(3), 803-806 (1966)
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