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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:
UNSPSC Code:
12352100
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

Related Categories

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

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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)
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

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