2-Iodo-4-nitrobenzoic acid
- Product Name
- 2-Iodo-4-nitrobenzoic acid
- CAS No.
- 89459-38-1
- Chemical Name
- 2-Iodo-4-nitrobenzoic acid
- Synonyms
- 2-Iodo-4-nitrobenzoic acid;Benzoic acid, 2-iodo-4-nitro-
- CBNumber
- CB82661449
- Molecular Formula
- C7H4INO4
- Formula Weight
- 293.02
- MOL File
- 89459-38-1.mol
2-Iodo-4-nitrobenzoic acid Property
- Melting point:
- 142 °C
- Boiling point:
- 402.8±35.0 °C(Predicted)
- Density
- 2.156±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C(protect from light)
- form
- solid
- pka
- 1.99±0.13(Predicted)
- Appearance
- Light yellow to yellow Solid
- InChI
- InChI=1S/C7H4INO4/c8-6-3-4(9(12)13)1-2-5(6)7(10)11/h1-3H,(H,10,11)
- InChIKey
- SQICTGFCQITYDT-UHFFFAOYSA-N
- SMILES
- C(O)(=O)C1=CC=C([N+]([O-])=O)C=C1I
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- I715625
- Product name
- 2-Iodo-4-nitrobenzoicAcid
- Packaging
- 50mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- I715625
- Product name
- 2-Iodo-4-nitrobenzoicAcid
- Packaging
- 500mg
- Price
- $155
- Updated
- 2021/12/16
- Product number
- 3262CC
- Product name
- 2-Iodo-4-nitrobenzoicacid
- Packaging
- 1g
- Price
- $176
- Updated
- 2021/12/16
- Product number
- HCH0058880
- Product name
- 2-IODO-4-NITROBENZOIC ACID
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $721.57
- Updated
- 2021/12/16
- Product number
- HCH0058880
- Product name
- 2-IODO-4-NITROBENZOIC ACID
- Purity
- 95.00%
- Packaging
- 2.5G
- Price
- $983.88
- Updated
- 2021/12/16
2-Iodo-4-nitrobenzoic acid Chemical Properties,Usage,Production
Synthesis
112391-34-1
89459-38-1
General procedure for the synthesis of 2-iodo-4-nitrobenzoic acid from the compound (CAS:112391-34-1): solid potassium iodide (55 g, 0.33 mol) was added in one go to a suspension of 2-iodo-4-nitrobenzoic acid I-1a (54.9 g, 0.18 mol) in water (250 mL) and glacial acetic acid (50 mL). Over the next 5-10 min, the solid gradually dissolved and the color of the solution changed from off-white to red. After stirring at 23 °C for 1 h, gaseous sulfur dioxide was passed into the reaction mixture until the red color disappeared and a light green suspension was formed. The solid product was collected by filtration and subsequently co-evaporated with toluene (3 x 250 mL) and finally dried under vacuum to give 2-iodo-4-nitrobenzoic acid I-1b (33 g, 64% yield).
References
[1] Collection of Czechoslovak Chemical Communications, 1989, vol. 54, # 4, p. 1012 - 1018
[2] Patent: US2004/122038, 2004, A1. Location in patent: Page 14
2-Iodo-4-nitrobenzoic acid Preparation Products And Raw materials
Raw materials
Preparation Products
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