Skip to Content
MilliporeSigma
All Photos(1)

Documents

219398

Sigma-Aldrich

3-Fluoroiodobenzene

99%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
FC6H4I
CAS Number:
1121-86-4
Molecular Weight:
222.00
EC Number:
214-339-9
MDL number:
MFCD00001044
UNSPSC Code:
12352100
PubChem Substance ID:
24853125
NACRES:
NA.22

assay

99%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.584 (lit.)

bp

77-78 °C/19 mmHg (lit.)

density

1.89 g/mL at 25 °C (lit.)

SMILES string

Fc1cccc(I)c1

InChI

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

InChI key

VSKSBSORLCDRHS-UHFFFAOYSA-N

Related Categories

General description

3-Fluoroiodobenzene participates in palladium-catalyzed hydroarylation of arylpropiolamides.

Application

3-Fluoroiodobenzene was used to prepare methyl 4-iodobenzo[b]thiophene-2-carboxylate, key intermediate for the synthesis of 4-substituted benzo[b]thiophene-2-carboxamidines.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

152.6 °F - closed cup

flash_point_c

67 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 3

1 of 3

2-Bromoiodobenzene 99%

Sigma-Aldrich

242616

2-Bromoiodobenzene

4-Iodotoluene 99%

Sigma-Aldrich

206555

4-Iodotoluene

4-Iodoanisole 98%

Sigma-Aldrich

I7608

4-Iodoanisole

M J Towle et al.
Cancer research, 53(11), 2553-2559 (1993-06-01)
Urokinase-type plasminogen activator (uPA) is an important mediator of cellular invasiveness. Specifically, cell surface receptor-bound uPA activates plasminogen to the potent general protease plasmin, which then degrades extracellular matrix or basement membrane either directly or via proteolytic activation of latent
A regio-and stereocontrolled method for preparing 3, 3-diarylacrylamides.
Hay LA and Mitchell D.
Tetrahedron Letters, 38(37), 6533-6536 (1997)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service