4-Nitroacetophenone Chemical Properties

Melting point:

75-78 °C(lit.)

Boiling point:

202 °C(lit.)

Density 

1.3450 (rough estimate)

refractive index 

1.5468 (estimate)

Flash point:

201-202°C

storage temp. 

Sealed in dry,Room Temperature

form 

Crystalline Powder

color 

Yellow

Water Solubility 

Insoluble in water.

BRN 

607777

InChIKey

YQYGPGKTNQNXMH-UHFFFAOYSA-N

CAS DataBase Reference

100-19-6(CAS DataBase Reference)

NIST Chemistry Reference

Acetophenone, 4'-nitro-(100-19-6)

EPA Substance Registry System

4-Nitroacetophenone (100-19-6)

Safety Information

Hazard Codes 

Xn

Risk Statements 

36-22

Safety Statements 

22-24/25

WGK Germany 

3

RTECS 

AM9627000

Hazard Note 

Harmful

HS Code 

29147090

MSDS

• Language:English Provider:1-(4-nitrophenyl)ethanone
• Language:English Provider:ACROS
• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

4-Nitroacetophenone Usage And Synthesis

Chemical Properties

The pure product is pale yellow crystal or needle crystal. Soluble in hot ethanol, ether and benzene, insoluble in water. 4-Nitroacetophenone is the raw material for the manufacture of synthomycin and chloramphenicol.

Uses

4''-Nitroacetophenone is used as a reagent in the synthesis of 4-Nitroacetophenone thiosemicarbazone derivatives and their copper(II) complexes which have potential anti-trypanosomal activity in vitro. Also used as a reagent in the synthesis of (R)-(4-Nitrophenyl)oxirane (N504430) and (S)-(4-Nitrophenyl)oxirane (N504435).

Preparation

In the presence of catalyst cobalt stearate, p-nitroethylbenzene is oxidized to synthesize 4-nitroacetophenone with air at 140-150°C and 0.2MPa pressure. The reaction product is washed with water, neutralized, centrifugally dehydrated, and dried to obtain a finished product.

Application

One of several alternative routes to synthetic chloroamphenicol uses 4-nitroacetophenone as starting material with a first-stage bromination to α-bromo-4-nitroacetophenone followed by buildup of the side chain. α-bromo-4-nitroacetophenone is the key precursor in the synthesis of the bronchodilator clenbuterol.

Definition

ChEBI: 4-nitroacetophenone is a member of the class of acetophenones that is acetophenone substituted at the para-position by a nitro group. It is a C-nitro compound and a member of acetophenones.

Synthesis Reference(s)

The Journal of Organic Chemistry, 48, p. 4634, 1983 DOI: 10.1021/jo00172a038
Synthetic Communications, 26, p. 291, 1996 DOI: 10.1080/00397919608003617

General Description

P-nitroacetophenone appears as yellow prisms or bright yellow powder. (NTP, 1992)

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

Flash point data for 4-Nitroacetophenone are not available. 4-Nitroacetophenone is probably combustible.

Purification Methods

Crystallise the ketone from EtOH or aqueous EtOH. [Beilstein 7 IV 657.]

4-Nitroacetophenone(100-19-6)Related Product Information

• 4'-Methoxyacetophenone
• 4'-Bromoacetophenone
• 4-Aminoacetophenone
• 3-Aminoacetophenone
• 4-Nitrobenzophenone
• 4'-Methylacetophenone
• 2-Nitroacetophenone
• Acetophenone
• 4'-Hydroxyacetophenone
• p-Nitrophenylacetonitrile
• L-PICEIN
• 4-Nitrophenylacetic acid
• 4'-Chloroacetophenone
• 3-Nitroacetophenone
• 4'-(Trifluoromethyl)acetophenone
• 4-NITROPHENYLACETYLENE
• 4-Nitrobenzyl alcohol
• 2-BROMO-2'-NITROACETOPHENONE