4-Iodo-3-nitrobenzoic acid
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
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
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
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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4-Iodo-3-nitrobenzoic acid(35674-27-2)Related Product Information
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