2-Nitroacetophenone

2-Nitroacetophenone Basic information
Product Name:2-Nitroacetophenone
Synonyms:Neighboring nitrobenzene ethyl ketone;2’-nitro-acetophenon;AKOS BBS-00003220;1-(2-nitrophenyl)ethanone;2'-NITROACETOPHENONE;2-NITROACETOPHENONE;LABOTEST-BB LT01895210;AURORA 14018
CAS:577-59-3
MF:C8H7NO3
MW:165.15
EINECS:209-414-8
Product Categories:Aromatic Acetophenones & Derivatives (substituted);Aromatics;C7 to C8;Carbonyl Compounds;Ketones;Miscellaneous Reagents;Carbonyl Compounds;pharmaceutical intermediates
Mol File:577-59-3.mol
2-Nitroacetophenone Structure
2-Nitroacetophenone Chemical Properties
Melting point 76-78 °C(lit.)
Boiling point 202 °C(lit.)
density 1.23
refractive index n20/D 1.55(lit.)
Fp >230 °F
storage temp. Sealed in dry,Room Temperature
solubility Chloroform, Ethyl Acetate
form Solid
color Brown
Water Solubility Insoluble
FreezingPoint 24.0 to 28.0 ℃
BRN 1102322
Stability:Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference577-59-3(CAS DataBase Reference)
NIST Chemistry ReferenceEthanone, 1-(2-nitrophenyl)-(577-59-3)
EPA Substance Registry System2-Nitroacetophenone (577-59-3)
Safety Information
Hazard Codes Xn
Risk Statements 22
Safety Statements 22-24/25
WGK Germany 3
RTECS AM9625000
Hazard Note Harmful
TSCA Yes
HS Code 29147090
MSDS Information
ProviderLanguage
o-Nitrophenyl methyl ketone English
SigmaAldrich English
ACROS English
ALFA English
2-Nitroacetophenone Usage And Synthesis
Chemical Propertiesyellow-green liquid or crystals. Soluble in alcohol, ether and chloroform, slightly soluble in water.
Uses2'-Nitroacetophenone is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and dyestuff. It is also used as a synthetic reagent. It is the sensitizer which can be used as pharmaceutical intermediates.
Uses2''-Nitroacetophenone (cas# 577-59-3) is a compound useful in organic synthesis. It is also used as an intermediate for photosensitive materials.?
Preparationo-Nitroacetophenone is synthesized from o-nitroethylbenzene by oxidation. Add o-nitroethylbenzene, decanoic acid and initiator azobisisobutyronitrile into the reaction tower, and at the same time slowly pass air into the tower, keep the pressure at 0.3-0.8MPa, and control the oxidation at 120-130°C to generate 2-Nitroacetophenone.
Synthesis Reference(s)The Journal of Organic Chemistry, 43, p. 3631, 1978 DOI: 10.1021/jo00412a058
Journal of the American Chemical Society, 105, p. 943, 1983 DOI: 10.1021/ja00342a050
Synthesis, p. 228, 1988 DOI: 10.1055/s-1988-27522
General DescriptionClear yellow liquid. Insoluble in water.
Air & Water ReactionsInsoluble in water.
Reactivity ProfileA nitrated ketone. Ketones are reactive with many acids and bases liberating heat and flammable gases (e.g., H2). The amount of heat may be sufficient to start a fire in the unreacted portion of the ketone. Ketones react with reducing agents such as hydrides, alkali metals, and nitrides to produce flammable gas (H2) and heat. Ketones are incompatible with isocyanates, aldehydes, cyanides, peroxides, and anhydrides. They react violently with aldehydes, HNO3, HNO3 + H2O2, and HClO4.
Fire Hazard2-Nitroacetophenone is combustible.
2-Nitrophenylacetonitrile Methylparaben Methyl 4'-Bromoacetophenone Parathion-methyl 4-Nitroacetophenone 2-BROMO-2'-NITROACETOPHENONE Acetophenone 2',4'-Dichloroacetophenone L-PICEIN 2-Bromoacetophenone Kresoxim-methyl 4'-Hydroxyacetophenone Thiophanate-methyl Dichloroacetonitrile 2'-Hydroxyacetophenone Methyl acrylate Nitrophenyl

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