Skip to Content
Merck
All Photos(1)

Key Documents

579157

Sigma-Aldrich

4-Iodobenzonitrile

97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
IC6H4CN
CAS Number:
Molecular Weight:
229.02
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

solid

mp

124-128 °C (lit.)

functional group

iodo
nitrile

SMILES string

Ic1ccc(cc1)C#N

InChI

1S/C7H4IN/c8-7-3-1-6(5-9)2-4-7/h1-4H

InChI key

XOKDXPVXJWTSRM-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

4-Iodobenzonitrile may be used in the synthesis of the following:
  • ethyl-4′-cyano-4-nitro[1,1′-biphenyl]-2-carboxylate via a multi-step reaction process
  • 2-(4-cyanophenyl)tellurophene obtained via Stille coupling with tellurophene
  • 2,5-bis(4-cyanophenyl)tellurophene obtained via Stille coupling with 2,5-bis(trimethylstannyl)tellurophene
  • ethyl-4′-cyano-6-{[(E)-phenylmethylidene]amino}[1,1′-biphenyl]-3-carboxylate via a multi-step reaction process

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

Nico Giordano et al.
Molecules (Basel, Switzerland), 24(10) (2019-05-30)
The crystal structure of 4-iodobenzonitrile, which is monoclinic (space group I2/a) under ambient conditions, contains chains of molecules linked through C≡N···I halogen-bonds. The chains interact through CH···I, CH···N and π-stacking contacts. The crystal structure remains in the same phase up
"Preparation and reactions of functionalized arylmagnesium reagents"
Jensen EA, et al.
Synthesis, 2002(04), 0565-0569 (2002)
"Synthesis of Nitro-Substituted Polyfunctional Biphenyls by Negishi Cross-Coupling of o-Nitroarylzinc Reagents"
Sapountzis I, et al.
Advanced Synthesis & Catalysis, 346(07), 709-712 (2004)
"Synthesis and stille cross-coupling reactions of 2-(tributylstannyl)-and 2, 5-bis (trimethylstannyl) tellurophene"
Sweat.PD and Stephens.EC
Synthesis, 2009(19), 3214-3218 (2009)

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