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HomeProduct name list4'-Nitroacetanilide

4'-Nitroacetanilide

Synonym(s):4′-Nitroacetanilide;Acetic acid 4-nitroanilide;N-Acetyl-4-nitroaniline

  • CAS NO.:104-04-1
  • Empirical Formula: C8H8N2O3
  • Molecular Weight: 180.16
  • MDL number: MFCD00007303
  • EINECS: 203-169-0
  • SAFETY DATA SHEET (SDS)
  • Update Date: 2023-04-23 13:52:06
4'-Nitroacetanilide Structural

What is 4'-Nitroacetanilide?

Chemical properties

solid

The Uses of 4'-Nitroacetanilide

Manufacture of nitraniline.

The Uses of 4'-Nitroacetanilide

4-Nitroacetanilide was used as a test substrate and its hydrolysis was determined by UV spectroscopic measurements. It was also used to prepare 4-aminoacetanilide.

What are the applications of Application

4-Nitroacetanilide is a synthetic intermediate

Preparation

Preparation of 4'-Nitroacetanilide from acetanilide.
Principle: Aromatic compounds can be conveniently nitrated by the use of the nitrating mixture, which is normally a mixture of concentrated nitric acid and concentrated sulphuric acid. The function of sulphuric acid is to convert nitric acid into a highly reactive, electrophilic, nitronium ion, NO2+, which is the effective nitrating agent. Nitration of activated aromatic compounds is carried out under milder condition whereas deactivated rings require drastic conditions. Activating groups are o, p-directing, while deactivating groups are m-directing for electrophilic substitution.
Reaction:
Preparation of 4'-Nitroacetanilide from acetanilide
Procedure: Take 0.5 g acetanilide in 0.6 ml glacial acetic acid and add 1 ml conc. H2SO4 in a beaker. Cool the mixture in ice salt bath (5-10°C). To this add a mixture of 0.2 ml conc. H2SO4 and 0.25 ml conc. HNO3 dropwise. Maintain the temperature below 10°C during addition. After addition is over allow the mixture to attain room temperature and leave it for 30 minutes. Pour the mixture on to crushed ice (20 g) with stirring. Filter the separated product and wash with cold water. Dry the product, record the practical yield and re-crystallize it.
Re-crystallization: Dissolve the crude product in minimum amount of ethyl alcohol in a beaker by heating on a water bath. Filter the hot solution and cool the filtrate. The crystals of the product separate out. Filter, dry and record the melting point and TLC (using toluene as solvent).

Synthesis Reference(s)

Journal of the American Chemical Society, 75, p. 5905, 1953 DOI: 10.1021/ja01119a037
Tetrahedron Letters, 28, p. 1669, 1987 DOI: 10.1016/S0040-4039(00)95389-9

Purification Methods

Precipitate the anilide from 80% H2SO4 by adding ice, then wash with water, and crystallise from aqueous EtOH. Dry it in air. [Beilstein 12 IV 1632.]

Properties of 4'-Nitroacetanilide

Melting point: 213-215 °C(lit.)
Boiling point: 312.97°C (rough estimate)
Density  1.340
refractive index  1.6180 (estimate)
storage temp.  Store below +30°C.
solubility  2.2g/l
form  Solid
pka 13.91±0.70(Predicted)
color  Yellow to green-yellow or green-brown
Water Solubility  2.2g/L(room temperature)
Merck  14,6581
BRN  2211962
Stability: Stable. Combustible. Incompatible with strong oxidizing agents.
CAS DataBase Reference 104-04-1(CAS DataBase Reference)
EPA Substance Registry System Acetamide, N-(4-nitrophenyl)- (104-04-1)

Safety information for 4'-Nitroacetanilide

Signal word Warning
Pictogram(s)
ghs
Exclamation Mark
Irritant
GHS07
GHS Hazard Statements H315:Skin corrosion/irritation
H319:Serious eye damage/eye irritation
H335:Specific target organ toxicity, single exposure;Respiratory tract irritation
Precautionary Statement Codes P261:Avoid breathing dust/fume/gas/mist/vapours/spray.
P264:Wash hands thoroughly after handling.
P264:Wash skin thouroughly after handling.
P271:Use only outdoors or in a well-ventilated area.
P280:Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Computed Descriptors for 4'-Nitroacetanilide

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