Skip to Content
Merck
All Photos(1)

Key Documents

219398

Sigma-Aldrich

3-Fluoroiodobenzene

99%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
FC6H4I
CAS Number:
Molecular Weight:
222.00
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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.)

functional group

fluoro
iodo

SMILES string

Fc1cccc(I)c1

InChI

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

InChI key

VSKSBSORLCDRHS-UHFFFAOYSA-N

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

152.6 °F - closed cup

Flash Point(C)

67 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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

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