Skip to Content
Merck
All Photos(1)

Key Documents

542903

Sigma-Aldrich

3-Chloro-4-fluoroiodobenzene

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
ClC6H3(F)I
CAS Number:
Molecular Weight:
256.44
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

refractive index

n20/D 1.604 (lit.)

bp

94-95 °C/15 mmHg (lit.)

density

2.008 g/mL at 25 °C (lit.)

functional group

chloro
fluoro
iodo

SMILES string

Fc1ccc(I)cc1Cl

InChI

1S/C6H3ClFI/c7-5-3-4(9)1-2-6(5)8/h1-3H

InChI key

OMASDGWBVAVFQZ-UHFFFAOYSA-N

General description

3-Chloro-4-fluoroiodobenzene, also known as 2-chloro-1-fluoro-4-iodobenzene [IUPAC name], is a polyhalobenzene. It participates in the synthesis of 3-carboxythiophene analogs.

Application

3-Chloro-4-fluoroiodobenzene may be used in the preparation of 2-chloro-1-(3,5-dimethoxyphenoxy)-4-iodobenzene by reacting with 3,5-dimethoxyphenol in the presence of cesium carbonate.

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)

230.0 °F - closed cup

Flash Point(C)

110 °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

Selectivity issues in the catalytic multiphase reduction of functionalized halogenated aromatics over Pd/C, Pt/C, and Raney-Ni
Evdokimova, Galina, et al.
Applied Catalysis A: General, 271.1, 129-136 (2004)
Fused thiophene derivatives as MEK inhibitors
Laing VE, et al.
Bioorganic & Medicinal Chemistry Letters, 22.1 , 472-475 (2012)
Synthesis of Phloroglucinol Monoaryl Ethers
Sherwood AM, et al.
Synthesis, 44.08, 1208-1212 (2012)

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