348-52-7

1-Fluoro-2-iodobenzene Chemical Structure
348-52-7

Chemical Structure

1-Fluoro-2-iodobenzene

Synonym(s): o-Iodofluorobenzene

  • CAS No.: 348-52-7
  • Formula:C6H4FI
  • Molecular Weight:222.00

IUPAC Name: 1-fluoro-2-iodobenzene

InChIKey: TYHUGKGZNOULKD-UHFFFAOYSA-N

SMILES: IC1=CC=CC=C1F

Biological Activity: 1-Fluoro-2-iodobenzene is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Cat. No. Product Name Purity Description Pricing
HY-34673
1-Fluoro-2-iodobenzene 99.43% 1-Fluoro-2-iodobenzene is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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HY-41755
2-Fluorophenol 99.84% 2-Fluorophenol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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HY-42121
4-Bromo-2-fluoro-1-iodobenzene 99.73% 4-Bromo-2-fluoro-1-iodobenzene (4-Bromo-2-fluoroiodobenzene) is a halogenated aromatic building block and also serves as the starting material for the synthesis of the selective FGFR2 inhibitor LHQ766 (HY-180794).
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HY-W004678
(2-Iodophenyl)methanol 99.81% (2-Iodophenyl)methanol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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HY-W007318
2-Iodoaniline 99.97% 2-Iodoaniline (2-Iodophenylamine) is an aniline derivative, and has potential hepatotoxic and nephrotoxic activity.
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HY-W007318S
2-Iodoaniline-13C6 2-Iodoaniline-13C6 is the 13C labeled 2-Iodoaniline.
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HY-W007846
2-Iodobenzaldehyde 99.95% 2-Iodobenzaldehyde (o-Iodobenzaldehyde) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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HY-W012392
3-Fluoro-4-iodopyridine 3-Fluoro-4-iodopyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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HY-Y0721S
3-Bromofluorobenzene-13C6 3-Bromofluorobenzene-13C6 is the 13C labeled 3-Bromofluorobenzene.
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HY-Y0747
Iodobenzene 99.91% Iodobenzene can undergo Ullmann coupling reaction on copper catalyst to generate biphenyl. Iodobenzene can undergo Suzuki reaction with phenylboronic acid to generate biphenyl.
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