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Thermo Scientific Chemicals
2-Fluoro-5-iodobenzoic acid, 97%
CAS: 124700-41-0 | C7H4FIO2 | 266.01 g/mol
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Chemical Identifiers
CAS124700-41-0
IUPAC Name2-fluoro-5-iodobenzoic acid
Molecular FormulaC7H4FIO2
InChI KeyQNNJHBNTHVHALE-UHFFFAOYSA-N
SMILESOC(=O)C1=C(F)C=CC(I)=C1
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Specifications
Specification Sheet
Specification SheetAssay (Aqueous acid-base Titration)≥96.0 to ≤104.0%
Appearance (Color)White to pale cream to cream to brown
FormCrystals or powder or crystalline powder
Assay (Silylated GC)≥96.0%
Melting Point (clear melt)159.0-168.0?C
2-Fluoro-5-iodobenzoic acid is one of the precursor molecules were shown to generate ETD reagents via ESI followed by CID. Starting material in the synthesis of 3, 6-disubstituted 2-pyridinecarboxamide(GK activators).
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2-Fluoro-5-iodobenzoic acid is one of the precursor molecules were shown to generate ETD reagents via ESI followed by CID. Starting material in the synthesis of 3, 6-disubstituted 2-pyridinecarboxamide(GK activators).
Solubility
Insoluble in water.
Notes
Light Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, light.
2-Fluoro-5-iodobenzoic acid is one of the precursor molecules were shown to generate ETD reagents via ESI followed by CID. Starting material in the synthesis of 3, 6-disubstituted 2-pyridinecarboxamide(GK activators).
Solubility
Insoluble in water.
Notes
Light Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, light.
RUO – Research Use Only
General References:
- Teng-Yi Huang,; Joshua F. Emory,; Richard A. J. O'Hair,; Scott A. McLuckey.Electron-Transfer Reagent Anion Formation via Electrospray Ionization and Collision-Induced Dissociation . Anal. Chem.,. 2006, 78 (21), 7387-7391.
- Morihiro Mitsuya; Kenji Kamata; Makoto Bamba; Hitomi Watanabe; Yasuhiro Sasaki; Kaori Sasaki; Sumika Ohyama; Hideka Hosaka; Yasufumi Nagata; Jun-ichi Eiki; Teruyuki Nishimura. Discovery of novel 3,6-disubstituted 2-pyridinecarboxamide derivatives as GK activators. Bioorganic & Medicinal Chemistry Letters. 2009, 19 (10), 2718-2721.