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219398

Sigma-Aldrich

3-Fluoroiodobenzene

99%

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

Quality Level

100

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

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

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

Regulatory Information

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A regio-and stereocontrolled method for preparing 3, 3-diarylacrylamides.
Hay LA and Mitchell D.
Tetrahedron Letters, 38(37), 6533-6536 (1997)
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

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