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2-Nitroacetophenone

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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
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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.)
Flash point:
>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 Reference
577-59-3(CAS DataBase Reference)
NIST Chemistry Reference
Ethanone, 1-(2-nitrophenyl)-(577-59-3)
EPA Substance Registry System
2-Nitroacetophenone (577-59-3)
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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

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2-Nitroacetophenone Usage And Synthesis

Chemical Properties

yellow-green liquid or crystals. Soluble in alcohol, ether and chloroform, slightly soluble in water.

Uses

2'-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.

Uses

2''-Nitroacetophenone (cas# 577-59-3) is a compound useful in organic synthesis. It is also used as an intermediate for photosensitive materials.?

Preparation

o-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 Description

Clear yellow liquid. Insoluble in water.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

A 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 Hazard

2-Nitroacetophenone is combustible.

2-Nitroacetophenone Preparation Products And Raw materials

Preparation Products

Raw materials

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