ChemicalBook--->CAS DataBase List--->914636-20-7

914636-20-7

914636-20-7 Structure

914636-20-7 Structure
IdentificationBack Directory
[Name]

4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID
[CAS]

914636-20-7
[Synonyms]

5-Carboxy-2-iodobenzotrifluoride
4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID
4-Iodo-3-(trifluoromethyl)benzoicacid99%
Benzoic acid, 4-iodo-3-(trifluoromethyl)-
4-Iodo-3-(trifluoromethyl)benzoic acid 99%
[Molecular Formula]

C8H4F3IO2
[MDL Number]

MFCD09258947
[MOL File]

914636-20-7.mol
[Molecular Weight]

316.02
Chemical PropertiesBack Directory
[Boiling point ]

311.7±42.0 °C(Predicted)
[density ]

2.005±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

crystalline needles
[pka]

3.59±0.10(Predicted)
[color ]

Tan/brown
[Sensitive ]

Light Sensitive/Air Sensitive
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID(914636-20-7)1HNMR
4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID(914636-20-7)FT-IR
Hazard InformationBack Directory
[Synthesis]

4-Amino-3-(Trifluoromethyl)Benzoic Acid 3-Trifluoromethyl-4-Aminobenzoic Acid

400-76-0

4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID

914636-20-7

General procedure for the synthesis of 4-iodo-3-(trifluoromethyl)benzoic acid from 3-trifluoromethyl-4-aminobenzoic acid: 4-amino-3-trifluoromethylbenzoic acid (1.8 g, 8.8 mmol) was suspended in 30 mL of hydrochloric acid. An aqueous solution (15 mL) of sodium nitrite (0.76 g, 11.0 mmol) was slowly added dropwise at 0°C. The reaction mixture was stirred at 0-10 °C for 30 min. Subsequently, an aqueous solution (25 mL) of potassium iodide (14.6 g, 88 mmol) was added dropwise. The mixture was stirred at room temperature for 1 hour. After completion of the reaction, the product was extracted with ethyl acetate (80 mL) and the organic layer was washed with brine (80 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by fast chromatography using a gradient elution with ethyl acetate/hexane, resulting in 4-iodo-3-(trifluoromethyl)benzoic acid (2.4 g, 86% yield) as a solid.LC-ES/MS analysis showed m/e 339.3 (M+23) and 315.0 (M-1).

[References]

[1] Patent: WO2007/140174, 2007, A2. Location in patent: Page/Page column 42
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