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219401

Sigma-Aldrich

2-Fluoroiodobenzene

99%, contains copper as stabilizer

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About This Item

Linear Formula:
FC6H4I
CAS Number:
348-52-7
Molecular Weight:
222.00
EC Number:
206-477-3
MDL number:
MFCD00001031
UNSPSC Code:
12352100
PubChem Substance ID:
24853126
NACRES:
NA.22

Assay

99%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.59 (lit.)

bp

188-189 °C (lit.)

mp

−41-−40 °C (lit.)

density

1.903 g/mL at 25 °C (lit.)

SMILES string

Fc1ccccc1I

InChI

1S/C6H4FI/c7-5-3-1-2-4-6(5)8/h1-4H

InChI key

TYHUGKGZNOULKD-UHFFFAOYSA-N

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Application

2-Fluoroiodobenzene was used in the synthesis of:
  • bridged biphenyl compounds, 1-fluoro-8-methylbiphenylene and 4-fluoro-5-methylfluorene
  • 2-acetyl-7-iodo-1-benzothiophene
  • chiral o-phosphanophenyl sulfoxides

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H315,H318

Precautionary Statements

P280 - P305 + P351 + P338

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

159.8 °F - closed cup

Flash Point(C)

71 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Pierre-Yves Michellys et al.
Bioorganic & medicinal chemistry letters, 14(6), 1593-1598 (2004-03-10)
The synthesis and in vitro characterization of novel RXR-selective ligands possessing various substituted 1-benzofuran or 1-benzothiophene moieties are described.
Long-range proton-fluorine spin-spin coupling in bridged biphenyls. Compelling evidence for a" through-space"(" direct") mechanism.
Gribble GW and Douglas Jr JR.
Journal of the American Chemical Society, 92(19), 5764-5765 (1970)
New chiral sulfoxide ligands possessing a phosphano or phosphanoamino functionality in palladium-catalyzed asymmetric allylic nucleophilic substitution reactions.
Hiroi K, et al.
Tetrahedron, 56(27), 4701-4710 (2000)

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