ChemicalBook--->CAS DataBase List--->447464-03-1

447464-03-1

447464-03-1 Structure

447464-03-1 Structure
IdentificationBack Directory
[Name]

2-FLUORO-3-IODOBENZOIC ACID
[CAS]

447464-03-1
[Synonyms]

BUTTPARK 122\01-03
2-FLUORO-3-IODOBENZOIC ACID
Benzoic acid, 2-fluoro-3-iodo-
[Molecular Formula]

C7H4FIO2
[MDL Number]

MFCD07774248
[MOL File]

447464-03-1.mol
[Molecular Weight]

266.01
Chemical PropertiesBack Directory
[Boiling point ]

331.0±27.0 °C(Predicted)
[density ]

2.074±0.06 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

crystalline powder
[pka]

2.92±0.10(Predicted)
[color ]

Faint brown
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[HS Code ]

2916399090
Spectrum DetailBack Directory
[Spectrum Detail]

2-FLUORO-3-IODOBENZOIC ACID(447464-03-1)1HNMR
2-FLUORO-3-IODOBENZOIC ACID(447464-03-1)1HNMR
2-FLUORO-3-IODOBENZOIC ACID(447464-03-1)19FNMR
Hazard InformationBack Directory
[Synthesis]

2-Fluoro-3-iodo-benzonitrile

211943-27-0

2-FLUORO-3-IODOBENZOIC ACID

447464-03-1

General procedure for the synthesis of 2-fluoro-3-iodobenzoic acid from 2-fluoro-3-iodobenzonitrile: A mixture of 2-fluoro-3-iodobenzonitrile (5.00 g, 20.2 mmol), dioxane (16 mL), and concentrated sulfuric acid (25 mL) was heated to 115 °C and reacted for 4 hours. After completion of the reaction, the mixture was cooled to room temperature and filtered to remove insoluble material. Water was added to the filtrate and the aqueous phase was extracted with ethyl acetate. The organic layers were combined, dried with anhydrous magnesium sulfate and concentrated under reduced pressure to give 2-fluoro-3-iodobenzoic acid (4.42 g, 82% yield) as a white solid. Mass spectrum (LRMS) m/z: 265 ([M-H]-). 1H-NMR (CDCl3) δ: 6.94-7.01 (m, 1H), 7.90-7.97 (m, 2H).

[References]

[1] Patent: EP2113503, 2009, A1. Location in patent: Page/Page column 32
[2] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 21, p. 6253 - 6257
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