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4-Iodo-3-nitrobenzoic acid

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4-Iodo-3-nitrobenzoic acid Basic information

Product Name:
4-Iodo-3-nitrobenzoic acid
Synonyms:
  • 4-IODO-3-NITROBENZOIC ACID
  • 3-Nitro-4-iodobenzoic acid
  • 4-Iodo-3-nitrobenzoic acid ,98%
  • Benzoic acid, 4-iodo-3-nitro-
  • 4-iodo-3-nitrobenzoicaci
CAS:
35674-27-2
MF:
C7H4INO4
MW:
293.02
EINECS:
670-347-6
Product Categories:
  • Benzoic acid series
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
Mol File:
35674-27-2.mol
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4-Iodo-3-nitrobenzoic acid Chemical Properties

Melting point:
208-211°C
Boiling point:
390.2±37.0 °C(Predicted)
Density 
2.156±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
form 
powder to crystal
pka
3.32±0.10(Predicted)
color 
Light orange to Yellow to Green
Water Solubility 
Insoluble in water.
Sensitive 
Light Sensitive
InChI
InChI=1S/C7H4INO4/c8-5-2-1-4(7(10)11)3-6(5)9(12)13/h1-3H,(H,10,11)
InChIKey
DNMTZLCNLAIKQC-UHFFFAOYSA-N
SMILES
C(O)(=O)C1=CC=C(I)C([N+]([O-])=O)=C1
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Safety Information

Risk Statements 
20/21/22-36/37/38
Safety Statements 
22-26-36/37/39
HS Code 
2916399090

MSDS

  • Language:English Provider:ALFA
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4-Iodo-3-nitrobenzoic acid Usage And Synthesis

Uses

4-Iodo-3-nitrobenzoic acid is used as a pharmaceutical intermediate.

Synthesis

1588-83-6

35674-27-2

Example 1 Preparation of 4-iodo-3-nitrobenzoic acid (Compound V): 45 g (0.25 mol) of 4-amino-3-nitrobenzoic acid, 400 mL of deionized water and 100 mL of concentrated hydrochloric acid were added to a reaction flask. Stirring was turned on and the reaction mixture was cooled to 0 to 5 °C before 50 mL of an aqueous solution containing 25.9 g (0.38 mol) of sodium nitrite was slowly added dropwise. Gradual dissolution of the solid was observed. After the dropwise addition was completed, the reaction was maintained at 0 to 5°C and continued for 1 hour. Subsequently, 200 mL of an aqueous solution containing 88 g (0.5 mol) of potassium iodide was slowly added dropwise at the same temperature. After completion of the dropwise addition, the reaction mixture was stirred at room temperature for 2 hours, during which time a solid precipitated. The solid product was collected by filtration, washed with deionized water and dried to give 65 g (0.22 mol) of 4-iodo-3-nitrobenzoic acid (compound V) in 89.7% yield.

References

[1] Patent: US2013/225810, 2013, A1. Location in patent: Paragraph 0081; 0082
[2] Tetrahedron, 2005, vol. 61, # 42, p. 10113 - 10121
[3] Tetrahedron Letters, 1997, vol. 38, # 46, p. 7963 - 7966
[4] Patent: WO2005/40157, 2005, A2. Location in patent: Page/Page column 67-68
[5] Patent: WO2010/62171, 2010, A2. Location in patent: Page/Page column 140

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