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344214

Sigma-Aldrich

2-Bromo-3′-nitroacetophenone

97%

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Synonym(s):
3′-Nitrophenacyl bromide
Linear Formula:
O2NC6H4COCH2Br
CAS Number:
Molecular Weight:
244.04
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

97%

form

solid

mp

90-96 °C (lit.)

SMILES string

[O-][N+](=O)c1cccc(c1)C(=O)CBr

InChI

1S/C8H6BrNO3/c9-5-8(11)6-2-1-3-7(4-6)10(12)13/h1-4H,5H2

InChI key

GZHPNIQBPGUSSX-UHFFFAOYSA-N

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This Item
245615534153D134406
2-Bromo-3′-nitroacetophenone 97%

344214

2-Bromo-3′-nitroacetophenone

2-Bromo-4′-nitroacetophenone 95%

245615

2-Bromo-4′-nitroacetophenone

mp

90-96 °C (lit.)

mp

94-99 °C (lit.)

mp

129-132 °C (lit.)

mp

124-127 °C (lit.)

form

solid

form

-

form

-

form

solid

General description

Debromination of 2-bromo-3′-nitroacetophenone in various solvents has been reported.

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.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible, corrosive hazardous materials

wgk_germany

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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2-Bromoacetophenone 98%

Sigma-Aldrich

115835

2-Bromoacetophenone

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)
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)

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